This variation has been flagged

None of the variant alleles match the reference allele

Select a location:
Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: 0.37 (T)
Location

This variation maps to 10 genomic locations; None selected

Evidence status

Synonyms

Archive dbSNP rs61036396

HGVS name

None

Variation displays