Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.25 (A)
Location

Chromosome 10:100101678 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs56552070, rs58359063

HGVS name

10:g.100101678G>A

This variation has assays on 10 chips - click the plus to show

About this variant

This variant overlaps 2 transcripts, has 2209 individual genotypes, is associated with 1 phenotype and is mentioned in 4 citations.

Variation displays