Original source

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

C/G | Ancestral: C | Ambiguity code: S | MAF: 0.48 (G)

Chromosome 7:30965828 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs61654257

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 6 transcripts, has 2772 sample genotypes and is mentioned in 1 citation.

Variant displays