Original source

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

Alleles
A/T | Ancestral: T | Ambiguity code: W | MAF: 0.07 (A)
Location

Chromosome 9:95191097 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs374952

This variant has 8 HGVS names - click the plus to show

About this variant

This variant overlaps 6 transcripts and has 2780 sample genotypes.

Variant displays