Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.27 (T)
Location

Chromosome 8:96161308 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs2514529

HGVS name

8:g.96161308C>T

About this variant

This variant overlaps 5 transcripts and has 2506 individual genotypes.

Variation displays