This variation has been flagged

Variation does not map to the genome

Original source

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

Alleles
A/T | Ambiguity code: W
Location

This variation has not been mapped

Evidence status

Synonyms

Archive dbSNP rs3810802

HGVS name

None

Variation displays