Original source

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

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

Chromosome 19:48394022 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

19:g.48394022C>G

About this variant

This variant overlaps 7 transcripts and has 2504 individual genotypes.

Variation displays