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rs200329677

From SNPedia

Orientationminus
Stabilizedminus
Make rs200329677(A;A)
Make rs200329677(A;G)
Make rs200329677(G;G)
ReferenceGRCh38.p7 38.3/151
Chromosome22
Position45973898
GeneWNT7B
is asnp
is mentioned by
dbSNPrs200329677
dbSNP (old)rs200329677
ClinGenrs200329677
ebirs200329677
HLIrs200329677
Exacrs200329677
Gnomadrs200329677
Varsomers200329677
Maprs200329677
PheGenIrs200329677
Biobankrs200329677
1000 genomesrs200329677
hgdprs200329677
ensemblrs200329677
gopubmedrs200329677
geneviewrs200329677
scholarrs200329677
googlers200329677
pharmgkbrs200329677
gwascentralrs200329677
openSNPrs200329677
23andMers200329677
23andMe allrs200329677
SNPshotrs200329677
SNPdbers200329677
MSV3drs200329677
GWAS Ctlgrs200329677
Max Magnitude

[PMID 29847655] Family-Based Genome-Wide Association Study of South Indian Pedigrees Supports WNT7B as a Central Corneal Thickness Locus.