Original source

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

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.30 (T)

Chromosome 7:130180556 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs57092735, rs2727834

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 6 transcripts and has 2506 sample genotypes.

Variant displays