Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.08 (C)
Location

Chromosome 10:111075351 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57125560, rs17186373

HGVS name

10:g.111075351A>C

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

Variation displays