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rs1005731602

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position184373564
GeneTHPO
is asnp
is mentioned by
dbSNPrs1005731602
dbSNP (old)rs1005731602
ClinGenrs1005731602
ebirs1005731602
HLIrs1005731602
Exacrs1005731602
Gnomadrs1005731602
Varsomers1005731602
Maprs1005731602
PheGenIrs1005731602
Biobankrs1005731602
1000 genomesrs1005731602
hgdprs1005731602
ensemblrs1005731602
gopubmedrs1005731602
geneviewrs1005731602
scholarrs1005731602
googlers1005731602
pharmgkbrs1005731602
gwascentralrs1005731602
openSNPrs1005731602
23andMers1005731602
23andMe allrs1005731602
SNP Nexus

SNPshotrs1005731602
SNPdbers1005731602
MSV3drs1005731602
GWAS Ctlgrs1005731602
Max Magnitude0
ClinVar
Risk rs1005731602(T;T)
Alt rs1005731602(T;T)
Reference Rs1005731602(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.184091352C>T
CLNSRC
CLNACC RCV000414736.1,