Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.29 (G)
Location

Chromosome 15:74719300 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR961724

Most severe consequence
Evidence status

Synonyms
HGVS name

15:g.74719300A>G

About this variant

This variant overlaps 10 transcripts, has 2508 individual genotypes and is mentioned in 79 citations.

Variation displays