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rs786205671

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205671(C;C)
Make rs786205671(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position65979910
GeneGUSB
is asnp
is mentioned by
dbSNPrs786205671
ebirs786205671
HLIrs786205671
Exacrs786205671
Varsomers786205671
Maprs786205671
PheGenIrs786205671
hapmaprs786205671
1000 genomesrs786205671
hgdprs786205671
ensemblrs786205671
gopubmedrs786205671
geneviewrs786205671
scholarrs786205671
googlers786205671
pharmgkbrs786205671
gwascentralrs786205671
openSNPrs786205671
23andMers786205671
23andMe allrs786205671
SNP Nexus

SNPshotrs786205671
SNPdbers786205671
MSV3drs786205671
GWAS Ctlgrs786205671
Max Magnitude0
ClinVar
Risk rs786205671(C;C)
Alt rs786205671(C;C)
Reference rs786205671(G;G)
Significance Probable-Pathogenic
Disease Non-immune hydrops fetalis
Variation info
Gene GUSB
CLNDBN Non-immune hydrops fetalis
Reversed 1
HGVS NC_000007.13:g.65444897C>G
CLNSRC
CLNACC RCV000170580.1,