Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.06 (C)
Location

Chromosome 9:95277061 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs13293318, rs57402214

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 6 transcripts and has 2771 sample genotypes.

Variant displays