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

Evidence status

Synonyms
HGVS name

None

About this variant

This variant has 1 individual genotype.

Variation displays