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rs387906339

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CC;CC) 0 common in clinvar
Make rs387906339(AG;AG)
Make rs387906339(AG;CC)
ReferenceGRCh38 38.1/141
Chromosome1
Position186313753
GenePRG4, TPR
is asnp
is mentioned by
dbSNPrs387906339
ebirs387906339
HLIrs387906339
Exacrs387906339
Varsomers387906339
Maprs387906339
PheGenIrs387906339
hapmaprs387906339
1000 genomesrs387906339
hgdprs387906339
ensemblrs387906339
gopubmedrs387906339
geneviewrs387906339
scholarrs387906339
googlers387906339
pharmgkbrs387906339
gwascentralrs387906339
openSNPrs387906339
23andMers387906339
23andMe allrs387906339
SNP Nexus

SNPshotrs387906339
SNPdbers387906339
MSV3drs387906339
GWAS Ctlgrs387906339
Max Magnitude0
ClinVar
Risk rs387906339(AG;AG)
Alt rs387906339(AG;AG)
Reference rs387906339(CC;CC)
Significance Pathogenic
Disease Camptodactyly arthropathy coxa vara pericarditis syndrome
Variation info
Gene PRG4 TPR
CLNDBN Camptodactyly arthropathy coxa vara pericarditis syndrome
Reversed 0
HGVS NC_000001.10:g.186282885_186282886delCCinsAG
CLNSRC OMIM Allelic Variant
CLNACC RCV000006009.2,