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rs786205668

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205668(A;A)
Make rs786205668(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position225100772
GeneDNAH14
is asnp
is mentioned by
dbSNPrs786205668
ebirs786205668
HLIrs786205668
Exacrs786205668
Varsomers786205668
Maprs786205668
PheGenIrs786205668
hapmaprs786205668
1000 genomesrs786205668
hgdprs786205668
ensemblrs786205668
gopubmedrs786205668
geneviewrs786205668
scholarrs786205668
googlers786205668
pharmgkbrs786205668
gwascentralrs786205668
openSNPrs786205668
23andMers786205668
23andMe allrs786205668
SNP Nexus

SNPshotrs786205668
SNPdbers786205668
MSV3drs786205668
GWAS Ctlgrs786205668
Max Magnitude0
ClinVar
Risk rs786205668(A;A)
Alt rs786205668(A;A)
Reference rs786205668(T;T)
Significance Probable-Pathogenic
Disease Non-immune hydrops fetalis
Variation info
Gene DNAH14
CLNDBN Non-immune hydrops fetalis
Reversed 0
HGVS NC_000001.10:g.225288474T>A
CLNSRC
CLNACC RCV000170575.1,