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rs749597090

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs749597090(C;T)
Make rs749597090(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome14
Position87945552
GeneGALC
is asnp
is mentioned by
dbSNPrs749597090
dbSNP (classic)rs749597090
ClinGenrs749597090
ebirs749597090
HLIrs749597090
Exacrs749597090
Gnomadrs749597090
Varsomers749597090
LitVarrs749597090
Maprs749597090
PheGenIrs749597090
Biobankrs749597090
1000 genomesrs749597090
hgdprs749597090
ensemblrs749597090
geneviewrs749597090
scholarrs749597090
googlers749597090
pharmgkbrs749597090
gwascentralrs749597090
openSNPrs749597090
23andMers749597090
SNPshotrs749597090
SNPdbers749597090
MSV3drs749597090
GWAS Ctlgrs749597090
Max Magnitude0
ClinVar
Risk rs749597090(T;T)
Alt rs749597090(T;T)
Reference Rs749597090(C;C)
Significance Probable-Pathogenic
Disease Galactosylceramide beta-galactosidase deficiency
Variation info
Gene GALC
CLNDBN Galactosylceramide beta-galactosidase deficiency
Reversed 0
HGVS NC_000014.8:g.88411896C>T
CLNSRC
CLNACC RCV000409892.1,