Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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

This variant has 10 HGVS names - click the plus to show

About this variant

This variant overlaps 13 transcripts and has 2511 sample genotypes.

Variant displays