Original source

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

C/G | Ancestral: G | Ambiguity code: S

Chromosome 5:41739892 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs661720

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 6 transcripts and has 3 sample genotypes.

Variant displays