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rs184280124

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs184280124(A;A)
Make rs184280124(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position18539333
GeneCACNB2, LOC105376439
is asnp
is mentioned by
dbSNPrs184280124
ebirs184280124
HLIrs184280124
Exacrs184280124
Varsomers184280124
Maprs184280124
PheGenIrs184280124
hapmaprs184280124
1000 genomesrs184280124
hgdprs184280124
ensemblrs184280124
gopubmedrs184280124
geneviewrs184280124
scholarrs184280124
googlers184280124
pharmgkbrs184280124
gwascentralrs184280124
openSNPrs184280124
23andMers184280124
23andMe allrs184280124
SNP Nexus

SNPshotrs184280124
SNPdbers184280124
MSV3drs184280124
GWAS Ctlgrs184280124
Max Magnitude0
ClinVar
Risk rs184280124(A;A)
Alt rs184280124(A;A)
Reference rs184280124(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CACNB2
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.18828262G>A
CLNSRC
CLNACC RCV000170872.3,