This variation has been flagged

Variation maps to 4 genomic locations

Select a location:
Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

G/A | Ancestral: G | Ambiguity code: R

This variation maps to 4 genomic locations; None selected

Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

HGVS name


About this variant

This variant overlaps 2 transcripts and is associated with 5 phenotypes.

Variation displays