Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.18 (A)
Location

Chromosome 19:55545805 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs74258005

HGVS name

19:g.55545805A>G

About this variant

This variant overlaps 3 transcripts and has 2514 individual genotypes.

Variation displays