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/C/G | Ambiguity code: N
Location

This variation has not been mapped

Synonyms

Archive dbSNP rs2621709

HGVS name

None

Variation displays