Original source

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

G/A/C | Ancestral: G | Ambiguity code: V | MAF: < 0.01 (A)

Chromosome 7:100825020 (forward strand) | View in location tab

Most severe consequence
Non coding transcript exon variant
Evidence status


Archive dbSNP rs1647621

HGVS names

This variant has 14 HGVS names - Show

About this variant

This variant overlaps 18 transcripts and has 2507 sample genotypes.

Variant displays