Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.29 (T)

Chromosome 6:3137960 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs57616209, rs17133178

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 11 transcripts and has 2845 sample genotypes.

Variant displays