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/C/G | Ambiguity code: V
Location

This variation has not been mapped

Evidence status

Synonyms

Archive dbSNP rs16822856, rs34301064

HGVS name

None

Variation displays