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rs16996652

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs16996652(A;T)
Make rs16996652(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position36300203
GeneMYH9
is asnp
is mentioned by
dbSNPrs16996652
ebirs16996652
HLIrs16996652
Exacrs16996652
Varsomers16996652
Maprs16996652
PheGenIrs16996652
hapmaprs16996652
1000 genomesrs16996652
hgdprs16996652
ensemblrs16996652
gopubmedrs16996652
geneviewrs16996652
scholarrs16996652
googlers16996652
pharmgkbrs16996652
gwascentralrs16996652
openSNPrs16996652
23andMers16996652
23andMe allrs16996652
SNP Nexus

SNPshotrs16996652
SNPdbers16996652
MSV3drs16996652
GWAS Ctlgrs16996652
Max Magnitude0

[PMID 19891592] Association Among Polymorphisms at MYH9, Environmental Factors, and Nonsyndromic Orofacial Clefts in Western China


ClinVar
Risk rs16996652(T;T)
Alt rs16996652(T;T)
Reference rs16996652(A;A)
Significance Non-pathogenic
Disease MYH9 related disorders
Variation info
Gene MYH9
CLNDBN MYH9 related disorders
Reversed 0
HGVS NC_000022.10:g.36696249A>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000032219.1,