Original source

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

Alleles
T/A|Ancestral: T|Ambiguity code: W|MAF: 0.42 (A)
Location

Chromosome 9:101434727 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs1634128

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 3 transcripts and has 2511 sample genotypes.

Variant displays