This variant has been flagged

None of the variant alleles match the reference allele

Select a location:
Original source

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

Alleles
G/C|Ancestral: G|Ambiguity code: S
Location

This variant maps to 8 genomic locations; None selected

Evidence status

Clinical significance

Synonyms

This variant has 3 synonyms - Show

HGVS name

None

About this variant

This variant is associated with 16 phenotypes and is mentioned in 1 citation.

Variant displays