Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.16 (C)
Location

Chromosome 9:124449165 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

9:g.124449165T>C

About this variant

This variant overlaps 2 transcripts and has 2507 individual genotypes.

Variation displays