Original source

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

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

Chromosome 11:77019346 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs10751272, rs56743266

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 13 transcripts and has 2511 sample genotypes.

Variant displays