Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: < 0.01 (T)
Location

Chromosome 7:44062690 (forward strand) | View in location tab

Most severe consequence

This variation has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 24 transcripts and has 2504 individual genotypes.

Variation displays