Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: 0.17 (G)
Location

Chromosome 1:203684896 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs60332666

This variant has 4 HGVS names - click the plus to show

1:g.203684896G>T
ENST00000341360.6:c.193+1498G>T
ENST00000367218.7:c.193+1498G>T
ENST00000357681.9:c.193+1498G>T

About this variant

This variant overlaps 3 transcripts, has 2511 sample genotypes, is associated with 1 phenotype and is mentioned in 2 citations.

Variant displays