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rs2071731

From SNPedia

Orientationplus
Stabilizedplus
Make rs2071731(A;A)
Make rs2071731(A;G)
Make rs2071731(G;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position36322813
GeneMYH9
is asnp
is mentioned by
dbSNPrs2071731
ebirs2071731
HLIrs2071731
Exacrs2071731
Varsomers2071731
Maprs2071731
PheGenIrs2071731
hapmaprs2071731
1000 genomesrs2071731
hgdprs2071731
ensemblrs2071731
gopubmedrs2071731
geneviewrs2071731
scholarrs2071731
googlers2071731
pharmgkbrs2071731
gwascentralrs2071731
openSNPrs2071731
23andMers2071731
23andMe allrs2071731
SNP Nexus

SNPshotrs2071731
SNPdbers2071731
MSV3drs2071731
GWAS Ctlgrs2071731
GMAF0.4233
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 19320731] Further evidence for the involvement of MYH9 in the etiology of non-syndromic cleft lip with or without cleft palate


[PMID 18716610OA-icon.png] Genomic screening identifies novel linkages and provides further evidence for a role of MYH9 in nonsyndromic cleft lip and palate.


[PMID 20124285OA-icon.png] Dense mapping of MYH9 localizes the strongest kidney disease associations to the region of introns 13 to 15.