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rs786205669

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205669(A;A)
Make rs786205669(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position52397636
GeneTHSD1
is asnp
is mentioned by
dbSNPrs786205669
ebirs786205669
HLIrs786205669
Exacrs786205669
Varsomers786205669
Maprs786205669
PheGenIrs786205669
hapmaprs786205669
1000 genomesrs786205669
hgdprs786205669
ensemblrs786205669
gopubmedrs786205669
geneviewrs786205669
scholarrs786205669
googlers786205669
pharmgkbrs786205669
gwascentralrs786205669
openSNPrs786205669
23andMers786205669
23andMe allrs786205669
SNP Nexus

SNPshotrs786205669
SNPdbers786205669
MSV3drs786205669
GWAS Ctlgrs786205669
Max Magnitude0
ClinVar
Risk rs786205669(A;A)
Alt rs786205669(A;A)
Reference rs786205669(G;G)
Significance Probable-Pathogenic
Disease Non-immune hydrops fetalis
Variation info
Gene THSD1
CLNDBN Non-immune hydrops fetalis
Reversed 1
HGVS NC_000013.10:g.52971771C>T
CLNSRC
CLNACC RCV000170576.1,