Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.37 (A)
Location

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

Most severe consequence
Evidence status

Synonyms

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

5:g.96766240A>G
ENST00000508608.3:c.2019+95A>G
ENST00000511049.3:c.1836+95A>G
ENST00000395813.3:c.1881+95A>G
ENST00000508579.3:c.1026+95A>G
ENST00000484552.3:c.1105+95A>G
ENST00000508830.3:c.2130+95A>G
ENST00000325674.9:c.1047+95A>G
ENST00000510756.3:c.2064+95A>G
ENST00000296754.5:c.2819-3012T>C
ENST00000511782.3:c.1839+95A>G
ENST00000510156.3:c.1881+95A>G
ENST00000395812.4:c.2007+95A>G
ENST00000509903.3:c.1776+95A>G
ENST00000309190.7:c.1815+95A>G
ENST00000341926.5:c.1881+95A>G
ENST00000510098.1:c.366+95A>G
ENST00000510500.3:c.1150+95A>G
ENST00000338252.5:c.1842+95A>G
ENST00000437034.4:c.1136+95A>G
ENST00000348386.5:n.1823+95A>G
ENST00000515663.3:c.1050+95A>G
ENST00000504465.3:c.1665+95A>G

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

Variation displays