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rs376780156

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs376780156(C;C)
Make rs376780156(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position156344676
GeneLOC105377674, SGCD
is asnp
is mentioned by
dbSNPrs376780156
ebirs376780156
HLIrs376780156
Exacrs376780156
Varsomers376780156
Maprs376780156
PheGenIrs376780156
hapmaprs376780156
1000 genomesrs376780156
hgdprs376780156
ensemblrs376780156
gopubmedrs376780156
geneviewrs376780156
scholarrs376780156
googlers376780156
pharmgkbrs376780156
gwascentralrs376780156
openSNPrs376780156
23andMers376780156
23andMe allrs376780156
SNP Nexus

SNPshotrs376780156
SNPdbers376780156
MSV3drs376780156
GWAS Ctlgrs376780156
Max Magnitude0
ClinVar
Risk rs376780156(C;C)
Alt rs376780156(C;C)
Reference rs376780156(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SGCD
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.155771686T>C
CLNSRC
CLNACC RCV000183902.1,