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
C/A|Ancestral: C|Ambiguity code: M
Location

This variant maps to 2 genomic locations; None selected

Evidence status

Clinical significance

Synonyms

LSDB 13818, NM_000157.2:c.1297G>T

HGVS name

None

About this variant

This variant is associated with 8 phenotypes and is mentioned in 3 citations.

Variant displays