Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.03 (G)
Location

Chromosome 19:44905218 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs1081102, rs495577

HGVS name

19:g.44905218A>G

About this variant

This variant overlaps 12 transcripts, has 2506 individual genotypes and is mentioned in 1 citation.

Variation displays