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rs373900644

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common/normal
(C;T) 3 Carrier of an orofaciodigital mutation
(T;T) 9 Orofaciodigital syndrome likely
ReferenceGRCh38.p2 38.2/147
Chromosome4
Position127663438
GeneINTU
is asnp
is mentioned by
dbSNPrs373900644
ebirs373900644
HLIrs373900644
Exacrs373900644
Varsomers373900644
Maprs373900644
PheGenIrs373900644
hapmaprs373900644
1000 genomesrs373900644
hgdprs373900644
ensemblrs373900644
gopubmedrs373900644
geneviewrs373900644
scholarrs373900644
googlers373900644
pharmgkbrs373900644
gwascentralrs373900644
openSNPrs373900644
23andMers373900644
23andMe allrs373900644
SNP Nexus

SNPshotrs373900644
SNPdbers373900644
MSV3drs373900644
GWAS Ctlgrs373900644
Max Magnitude9
see [PMID 27158779]