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rs786205490

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205490(G;T)
Make rs786205490(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position42384483
GeneCAPN3, LOC105370794
is asnp
is mentioned by
dbSNPrs786205490
ebirs786205490
HLIrs786205490
Exacrs786205490
Varsomers786205490
Maprs786205490
PheGenIrs786205490
hapmaprs786205490
1000 genomesrs786205490
hgdprs786205490
ensemblrs786205490
gopubmedrs786205490
geneviewrs786205490
scholarrs786205490
googlers786205490
pharmgkbrs786205490
gwascentralrs786205490
openSNPrs786205490
23andMers786205490
23andMe allrs786205490
SNP Nexus

SNPshotrs786205490
SNPdbers786205490
MSV3drs786205490
GWAS Ctlgrs786205490
Max Magnitude0
ClinVar
Risk rs786205490(T;T)
Alt rs786205490(T;T)
Reference rs786205490(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CAPN3
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.42676681G>T
CLNSRC
CLNACC RCV000171231.1,