This variation maps to 2 locations

Select a location:
Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: < 0.01 (A)
Location

This variation maps to 2 genomic locations; None selected

Evidence status

HGVS name

None

About this variant

This variant has 1092 individual genotypes and is mentioned in 1 citation.

Variation displays