Original source

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

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

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

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