Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.28 (G)
Location

Chromosome 19:41966222 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59923054

HGVS name

19:g.41966222G>A

This variation has assays on 6 chips - click the plus to show

About this variant

This variant overlaps 5 transcripts and has 3696 individual genotypes.

Variation displays