Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.39 (A)
Location

Chromosome 5:96766240 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

This variant has 23 HGVS names - click the plus to show

5:g.96766240A>G
ENST00000508608.5:c.2019+95A>G
ENST00000395813.5:c.1881+95A>G
ENST00000511049.5:c.1836+95A>G
ENST00000508579.5:c.1026+95A>G
ENST00000484552.5:c.1105+95A>G
ENST00000508830.5:c.2130+95A>G
ENST00000325674.11:c.1047+95A>G
ENST00000296754.7:c.2819-3012T>C
ENST00000510756.5:c.2064+95A>G
ENST00000511782.5:c.1839+95A>G
ENST00000510156.5:c.1881+95A>G
ENST00000395812.6:c.2007+95A>G
ENST00000509903.5:c.1776+95A>G
ENST00000309190.9:c.1815+95A>G
ENST00000341926.7:c.1881+95A>G
ENST00000510098.1:c.366+95A>G
ENST00000510500.5:c.1150+95A>G
ENST00000338252.7:c.1842+95A>G
ENST00000437034.6:c.1136+95A>G
ENST00000348386.7:n.1823+95A>G
ENST00000515663.5:c.1050+95A>G
ENST00000504465.5:c.1665+95A>G

This variant has assays on 10 chips - click the plus to show

About this variant

This variant overlaps 23 transcripts, has 2621 sample genotypes, is associated with 2 phenotypes and is mentioned in 8 citations.

Variant displays