Original source

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

C/G | Ancestral: C | Ambiguity code: S | MAF: 0.29 (G)

Chromosome 7:30962266 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs36206345, rs28371550

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 2 transcripts and has 2509 sample genotypes.

Variant displays