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rs786205673

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205673(C;T)
Make rs786205673(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position65980313
GeneGUSB
is asnp
is mentioned by
dbSNPrs786205673
ebirs786205673
HLIrs786205673
Exacrs786205673
Varsomers786205673
Maprs786205673
PheGenIrs786205673
hapmaprs786205673
1000 genomesrs786205673
hgdprs786205673
ensemblrs786205673
gopubmedrs786205673
geneviewrs786205673
scholarrs786205673
googlers786205673
pharmgkbrs786205673
gwascentralrs786205673
openSNPrs786205673
23andMers786205673
23andMe allrs786205673
SNP Nexus

SNPshotrs786205673
SNPdbers786205673
MSV3drs786205673
GWAS Ctlgrs786205673
Max Magnitude0
ClinVar
Risk rs786205673(T;T)
Alt rs786205673(T;T)
Reference rs786205673(C;C)
Significance Probable-Pathogenic
Disease Non-immune hydrops fetalis
Variation info
Gene GUSB
CLNDBN Non-immune hydrops fetalis
Reversed 1
HGVS NC_000007.13:g.65445300G>A
CLNSRC
CLNACC RCV000170584.1,