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rs772219642

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs772219642(G;T)
Make rs772219642(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position180619298
GeneCCDC39
is asnp
is mentioned by
dbSNPrs772219642
dbSNP (classic)rs772219642
ClinGenrs772219642
ebirs772219642
HLIrs772219642
Exacrs772219642
Gnomadrs772219642
Varsomers772219642
LitVarrs772219642
Maprs772219642
PheGenIrs772219642
Biobankrs772219642
1000 genomesrs772219642
hgdprs772219642
ensemblrs772219642
geneviewrs772219642
scholarrs772219642
googlers772219642
pharmgkbrs772219642
gwascentralrs772219642
openSNPrs772219642
23andMers772219642
SNPshotrs772219642
SNPdbers772219642
MSV3drs772219642
GWAS Ctlgrs772219642
Max Magnitude0
ClinVar
Risk rs772219642(T;T)
Alt rs772219642(T;T)
Reference Rs772219642(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene CCDC39
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.180337086G>T
CLNSRC
CLNACC RCV000479757.1,