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rs145580093

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs145580093(C;C)
Make rs145580093(C;T)
ReferenceGRCh38.p7 38.3/149
Chromosome14
Position87986582
GeneGALC
is asnp
is mentioned by
dbSNPrs145580093
dbSNP (classic)rs145580093
ClinGenrs145580093
ebirs145580093
HLIrs145580093
Exacrs145580093
Gnomadrs145580093
Varsomers145580093
LitVarrs145580093
Maprs145580093
PheGenIrs145580093
Biobankrs145580093
1000 genomesrs145580093
hgdprs145580093
ensemblrs145580093
geneviewrs145580093
scholarrs145580093
googlers145580093
pharmgkbrs145580093
gwascentralrs145580093
openSNPrs145580093
23andMers145580093
SNPshotrs145580093
SNPdbers145580093
MSV3drs145580093
GWAS Ctlgrs145580093
Max Magnitude0
ClinVar
Risk rs145580093(C;C)
Alt rs145580093(C;C)
Reference Rs145580093(T;T)
Significance Pathogenic
Disease not provided not specified
Variation info
Gene GALC
CLNDBN not provided not specified
Reversed 0
HGVS NC_000014.8:g.88452926T>C
CLNSRC
CLNACC RCV000078201.6, RCV000259045.1,