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rs863224933

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863224933(-;GAGGTGT)
Make rs863224933(GAGGTGT;GAGGTGT)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position39665383
GeneTCAP
is asnp
is mentioned by
dbSNPrs863224933
dbSNP (old)rs863224933
ClinGenrs863224933
ebirs863224933
HLIrs863224933
Exacrs863224933
Varsomers863224933
Maprs863224933
PheGenIrs863224933
Biobankrs863224933
1000 genomesrs863224933
hgdprs863224933
ensemblrs863224933
gopubmedrs863224933
geneviewrs863224933
scholarrs863224933
googlers863224933
pharmgkbrs863224933
gwascentralrs863224933
openSNPrs863224933
23andMers863224933
23andMe allrs863224933
SNP Nexus

SNPshotrs863224933
SNPdbers863224933
MSV3drs863224933
GWAS Ctlgrs863224933
Max Magnitude0
ClinVar
Risk rs863224933(GAGGTGT;GAGGTGT)
Alt rs863224933(GAGGTGT;GAGGTGT)
Reference Rs863224933(-;-)
Significance Probable-Pathogenic
Disease Limb-girdle muscular dystrophy
Variation info
Gene TCAP
CLNDBN Limb-girdle muscular dystrophy, type 2G
Reversed 0
HGVS NC_000017.10:g.37821636_37821637insGAGGTGT
CLNSRC
CLNACC RCV000196697.1,