Original source

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

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

Chromosome 12:48787246 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs61196882

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 5 transcripts and has 2511 sample genotypes.

Variant displays