This variation has been flagged

Variation maps to 8 genomic locations

Select a location:
Original source

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

Alleles
C/G/T | Ancestral: G | Ambiguity code: B
Location

This variation maps to 8 genomic locations; None selected

Evidence status

Synonyms

Archive dbSNP rs16822856, rs34301064

HGVS name

None

Variation displays