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rs786205674

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205674(A;G)
Make rs786205674(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position65967798
GeneGUSB
is asnp
is mentioned by
dbSNPrs786205674
ebirs786205674
HLIrs786205674
Exacrs786205674
Varsomers786205674
Maprs786205674
PheGenIrs786205674
hapmaprs786205674
1000 genomesrs786205674
hgdprs786205674
ensemblrs786205674
gopubmedrs786205674
geneviewrs786205674
scholarrs786205674
googlers786205674
pharmgkbrs786205674
gwascentralrs786205674
openSNPrs786205674
23andMers786205674
23andMe allrs786205674
SNP Nexus

SNPshotrs786205674
SNPdbers786205674
MSV3drs786205674
GWAS Ctlgrs786205674
Max Magnitude0
ClinVar
Risk rs786205674(G;G)
Alt rs786205674(G;G)
Reference rs786205674(A;A)
Significance Probable-Pathogenic
Disease Non-immune hydrops fetalis
Variation info
Gene GUSB
CLNDBN Non-immune hydrops fetalis
Reversed 1
HGVS NC_000007.13:g.65432785T>C
CLNSRC
CLNACC RCV000170585.1,