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rs9619601

From SNPedia

Orientationplus
Stabilizedplus
Make rs9619601(A;A)
Make rs9619601(A;G)
Make rs9619601(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome22
Position36304129
GeneMYH9
is asnp
is mentioned by
dbSNPrs9619601
dbSNP (classic)rs9619601
ClinGenrs9619601
ebirs9619601
HLIrs9619601
Exacrs9619601
Gnomadrs9619601
Varsomers9619601
LitVarrs9619601
Maprs9619601
PheGenIrs9619601
Biobankrs9619601
1000 genomesrs9619601
hgdprs9619601
ensemblrs9619601
geneviewrs9619601
scholarrs9619601
googlers9619601
pharmgkbrs9619601
gwascentralrs9619601
openSNPrs9619601
23andMers9619601
SNPshotrs9619601
SNPdbers9619601
MSV3drs9619601
GWAS Ctlgrs9619601
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 29207917] Functional Effects of SNPs in MYH9 and Risks of Nonsyndromic Orofacial Clefts.