This variant has been flagged

Variation has more than 3 different alleles

Select a location:
Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/A/G/T | Ambiguity code: N | MAF: 0.02 (A)
Location

This variant maps to 7 genomic locations; None selected

Evidence status

This variant has 2 synonyms - click the plus to show

HGVS name

None

About this variant

This variant has 2505 sample genotypes.

Variant displays