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rs727503422

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727503422(A;A)
Make rs727503422(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position156508703
GeneSGCD
is asnp
is mentioned by
dbSNPrs727503422
ebirs727503422
HLIrs727503422
Exacrs727503422
Varsomers727503422
Maprs727503422
PheGenIrs727503422
hapmaprs727503422
1000 genomesrs727503422
hgdprs727503422
ensemblrs727503422
gopubmedrs727503422
geneviewrs727503422
scholarrs727503422
googlers727503422
pharmgkbrs727503422
gwascentralrs727503422
openSNPrs727503422
23andMers727503422
23andMe allrs727503422
SNP Nexus

SNPshotrs727503422
SNPdbers727503422
MSV3drs727503422
GWAS Ctlgrs727503422
Max Magnitude0
ClinVar
Risk rs727503422(A;A)
Alt rs727503422(A;A)
Reference rs727503422(G;G)
Significance Probable-Pathogenic
Disease Limb-girdle muscular dystrophy
Variation info
Gene SGCD
CLNDBN Limb-girdle muscular dystrophy
Reversed 0
HGVS NC_000005.9:g.155935713G>A
CLNSRC
CLNACC RCV000151871.1,