Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: 0.07 (T)
Location

Chromosome 14:21635045 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

14:g.21635045G>T

About this variant

This variant overlaps 1 transcript and has 1095 individual genotypes.

Variation displays