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rs786205667

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205667(C;C)
Make rs786205667(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position172441964
GeneC1orf105, LOC102724528, PIGC
is asnp
is mentioned by
dbSNPrs786205667
ebirs786205667
HLIrs786205667
Exacrs786205667
Varsomers786205667
Maprs786205667
PheGenIrs786205667
hapmaprs786205667
1000 genomesrs786205667
hgdprs786205667
ensemblrs786205667
gopubmedrs786205667
geneviewrs786205667
scholarrs786205667
googlers786205667
pharmgkbrs786205667
gwascentralrs786205667
openSNPrs786205667
23andMers786205667
23andMe allrs786205667
SNP Nexus

SNPshotrs786205667
SNPdbers786205667
MSV3drs786205667
GWAS Ctlgrs786205667
Max Magnitude0
ClinVar
Risk rs786205667(C;C)
Alt rs786205667(C;C)
Reference rs786205667(T;T)
Significance Probable-Pathogenic
Disease Non-immune hydrops fetalis
Variation info
Gene C1orf105 PIGC
CLNDBN Non-immune hydrops fetalis
Reversed 1
HGVS NC_000001.10:g.172411104A>G
CLNSRC
CLNACC RCV000170570.2,