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rs560020203

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs560020203(C;T)
Make rs560020203(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position18538188
GeneCACNB2, LOC105376439
is asnp
is mentioned by
dbSNPrs560020203
ebirs560020203
HLIrs560020203
Exacrs560020203
Varsomers560020203
Maprs560020203
PheGenIrs560020203
hapmaprs560020203
1000 genomesrs560020203
hgdprs560020203
ensemblrs560020203
gopubmedrs560020203
geneviewrs560020203
scholarrs560020203
googlers560020203
pharmgkbrs560020203
gwascentralrs560020203
openSNPrs560020203
23andMers560020203
23andMe allrs560020203
SNP Nexus

SNPshotrs560020203
SNPdbers560020203
MSV3drs560020203
GWAS Ctlgrs560020203
Max Magnitude0
ClinVar
Risk rs560020203(A,T;A,T)
Alt rs560020203(A,T;A,T)
Reference rs560020203(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CACNB2
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.18827117C>A
CLNSRC
CLNACC RCV000170867.2,