This variant has been flagged

Variation does not map to the genome

Original source

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

Alleles
A/T|Ambiguity code: W
Location

This variant has not been mapped

Evidence status

Synonyms

Archive dbSNP rs16978767, rs3199741

HGVS name

None

Variant displays