This variant maps to 2 locations

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Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
A/T|Ancestral: T|Ambiguity code: W|MAF: 0.09 (T)
Location

This variant maps to 2 genomic locations; None selected

Evidence status

Synonyms

Archive dbSNP rs118164267

HGVS name

None

About this variant

This variant overlaps 1 regulatory feature, has 2801 sample genotypes and is mentioned in 1 citation.

Variant displays