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rs187043152

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs187043152(A;A)
Make rs187043152(A;G)
ReferenceGRCh38 38.1/142
Chromosome8
Position105801714
is asnp
is mentioned by
dbSNPrs187043152
ebirs187043152
HLIrs187043152
Exacrs187043152
Varsomers187043152
Maprs187043152
PheGenIrs187043152
hapmaprs187043152
1000 genomesrs187043152
hgdprs187043152
ensemblrs187043152
gopubmedrs187043152
geneviewrs187043152
scholarrs187043152
googlers187043152
pharmgkbrs187043152
gwascentralrs187043152
openSNPrs187043152
23andMers187043152
23andMe allrs187043152
SNP Nexus

SNPshotrs187043152
SNPdbers187043152
MSV3drs187043152
GWAS Ctlgrs187043152
Max Magnitude0
ClinVar
Risk rs187043152(A,T;A,T)
Alt rs187043152(A,T;A,T)
Reference rs187043152(G;G)
Significance Pathogenic
Disease Tetralogy of Fallot 46
Variation info
Gene ZFPM2 ZFPM2-AS1
CLNDBN Tetralogy of Fallot 46,XY sex reversal 9
Reversed 0
HGVS NC_000008.10:g.106813942G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000032716.3, RCV000144723.2,