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rs397517237

From SNPedia

Orientationplus
Geno Mag Summary
(TGT;TGT) 0 common in clinvar
Make rs397517237(-;-)
Make rs397517237(-;GTT)
Make rs397517237(GTT;GTT)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position74112025
GeneVCL
is asnp
is mentioned by
dbSNPrs397517237
ebirs397517237
HLIrs397517237
Exacrs397517237
Varsomers397517237
Maprs397517237
PheGenIrs397517237
hapmaprs397517237
1000 genomesrs397517237
hgdprs397517237
ensemblrs397517237
gopubmedrs397517237
geneviewrs397517237
scholarrs397517237
googlers397517237
pharmgkbrs397517237
gwascentralrs397517237
openSNPrs397517237
23andMers397517237
23andMe allrs397517237
SNP Nexus

SNPshotrs397517237
SNPdbers397517237
MSV3drs397517237
GWAS Ctlgrs397517237
Max Magnitude0
ClinVar
Risk rs397517237(;)
Alt rs397517237(;)
Reference rs397517237(TGT;TGT)
Significance Probable-Pathogenic
Disease not specified Dilated cardiomyopathy Cardiomyopathy Dilated cardiomyopathy 1W
Variation info
Gene VCL
CLNDBN not specified Dilated cardiomyopathy Cardiomyopathy Dilated cardiomyopathy 1W
Reversed 0
HGVS NC_000010.10:g.75871783_75871785delGTT
CLNSRC
CLNACC RCV000038819.3, RCV000171847.1, RCV000184004.1, RCV000225812.1,