Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S | MAF: 0.02 (C)
Location

Chromosome 19:14091191 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

19:g.14091191G>C

About this variant

This variant overlaps 10 transcripts and has 1092 individual genotypes.

Variation displays