Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.31 (T)
Location

Chromosome 6:43515061 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs9462901

HGVS names

This variant has 14 HGVS names - Show

About this variant

This variant overlaps 28 transcripts and has 2507 sample genotypes.

Variant displays