This variation maps to 2 locations

Select a location:
Original source

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

Alleles
A/C/G/T | Ambiguity code: N
Location

This variation maps to 2 genomic locations; None selected

Evidence status

This variation has 4 synonyms - click the plus to show

HGVS name

None

About this variant

This variant has 2 individual genotypes.

Variation displays