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rs1801505

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1801505(A;A)
Make rs1801505(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position42384492
GeneCAPN3, LOC105370794
is asnp
is mentioned by
dbSNPrs1801505
ebirs1801505
HLIrs1801505
Exacrs1801505
Varsomers1801505
Maprs1801505
PheGenIrs1801505
hapmaprs1801505
1000 genomesrs1801505
hgdprs1801505
ensemblrs1801505
gopubmedrs1801505
geneviewrs1801505
scholarrs1801505
googlers1801505
pharmgkbrs1801505
gwascentralrs1801505
openSNPrs1801505
23andMers1801505
23andMe allrs1801505
SNP Nexus

SNPshotrs1801505
SNPdbers1801505
MSV3drs1801505
GWAS Ctlgrs1801505
Max Magnitude0
ClinVar
Risk rs1801505(A;A)
Alt rs1801505(A;A)
Reference rs1801505(G;G)
Significance Pathogenic
Disease not specified Limb-girdle muscular dystrophy
Variation info
Gene CAPN3
CLNDBN not specified Limb-girdle muscular dystrophy, type 2A
Reversed 0
HGVS NC_000015.9:g.42676690G>A; NC_000015.9:g.42676690G>T
CLNSRC
CLNACC RCV000175518.1, RCV000196140.1,