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rs747753388

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs747753388(C;T)
Make rs747753388(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position144682908
GeneTPK1
is asnp
is mentioned by
dbSNPrs747753388
ClinGenrs747753388
ebirs747753388
HLIrs747753388
Exacrs747753388
Varsomers747753388
Maprs747753388
PheGenIrs747753388
hapmaprs747753388
1000 genomesrs747753388
hgdprs747753388
ensemblrs747753388
gopubmedrs747753388
geneviewrs747753388
scholarrs747753388
googlers747753388
pharmgkbrs747753388
gwascentralrs747753388
openSNPrs747753388
23andMers747753388
23andMe allrs747753388
SNP Nexus

SNPshotrs747753388
SNPdbers747753388
MSV3drs747753388
GWAS Ctlgrs747753388
Max Magnitude0
ClinVar
Risk rs747753388(T;T)
Alt rs747753388(T;T)
Reference Rs747753388(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TPK1
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.144380001C>T
CLNSRC
CLNACC RCV000197327.1,