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 (G)
Location

Chromosome 10:74848766 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57852570

This variation has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 5 transcripts and has 2665 individual genotypes.

Variation displays