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rs786205670

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205670(-;-)
Make rs786205670(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome20
Position45892875
GeneCTSA, NEURL2
is asnp
is mentioned by
dbSNPrs786205670
ebirs786205670
HLIrs786205670
Exacrs786205670
Varsomers786205670
Maprs786205670
PheGenIrs786205670
hapmaprs786205670
1000 genomesrs786205670
hgdprs786205670
ensemblrs786205670
gopubmedrs786205670
geneviewrs786205670
scholarrs786205670
googlers786205670
pharmgkbrs786205670
gwascentralrs786205670
openSNPrs786205670
23andMers786205670
23andMe allrs786205670
SNP Nexus

SNPshotrs786205670
SNPdbers786205670
MSV3drs786205670
GWAS Ctlgrs786205670
Max Magnitude0
ClinVar
Risk rs786205670(;)
Alt rs786205670(;)
Reference rs786205670(C;C)
Significance Probable-Pathogenic
Disease Non-immune hydrops fetalis
Variation info
Gene CTSA NEURL2
CLNDBN Non-immune hydrops fetalis
Reversed 0
HGVS NC_000020.10:g.44521514delC
CLNSRC
CLNACC RCV000170578.1,