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rs391695

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs391695(A;A)
Make rs391695(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position164104554
GeneLOC100289273
is asnp
is mentioned by
dbSNPrs391695
ebirs391695
HLIrs391695
Exacrs391695
Varsomers391695
Maprs391695
PheGenIrs391695
hapmaprs391695
1000 genomesrs391695
hgdprs391695
ensemblrs391695
gopubmedrs391695
geneviewrs391695
scholarrs391695
googlers391695
pharmgkbrs391695
gwascentralrs391695
openSNPrs391695
23andMers391695
23andMe allrs391695
SNP Nexus

SNPshotrs391695
SNPdbers391695
MSV3drs391695
GWAS Ctlgrs391695
GMAF0.007805
Max Magnitude0
? (A;A) (A;G) (G;G) 28
OMIM603176
DescSCHIZOPHRENIA 7; SCZD7
Variant
Relatedalso
OMIM607415
DescG30 GENE
Variant
Relatedalso