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rs7795356

From SNPedia

Orientationplus
Stabilizedplus
Make rs7795356(C;C)
Make rs7795356(C;T)
Make rs7795356(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position116576975
GeneLOC100996266
is asnp
is mentioned by
dbSNPrs7795356
ebirs7795356
HLIrs7795356
Exacrs7795356
Varsomers7795356
Maprs7795356
PheGenIrs7795356
hapmaprs7795356
1000 genomesrs7795356
hgdprs7795356
ensemblrs7795356
gopubmedrs7795356
geneviewrs7795356
scholarrs7795356
googlers7795356
pharmgkbrs7795356
gwascentralrs7795356
openSNPrs7795356
23andMers7795356
23andMe allrs7795356
SNP Nexus

SNPshotrs7795356
SNPdbers7795356
MSV3drs7795356
GWAS Ctlgrs7795356
GMAF0.1777
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 23743525OA-icon.png] Association study of genetic variants on chromosome 7q31 with susceptibility to normal tension glaucoma in a Japanese population