Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 11:64751597 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CS032423

Most severe consequence
Clinical significance

Synonyms

LSDB 15737

This variation has 4 HGVS names - click the plus to show

11:g.64751597C>T
ENST00000462303.1:n.151G>A
ENST00000164139.3:c.1827G>A
ENST00000377432.5:c.1563G>A

Variation displays