Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.21 (C)
Location

Chromosome 9:95220429 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57933405, rs28498656

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

About this variant

This variant overlaps 6 transcripts and has 2510 individual genotypes.

Variation displays