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rs746607723

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs746607723(A;A)
Make rs746607723(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position31859797
GeneNEU1
is asnp
is mentioned by
dbSNPrs746607723
ClinGenrs746607723
ebirs746607723
HLIrs746607723
Exacrs746607723
Varsomers746607723
Maprs746607723
PheGenIrs746607723
hapmaprs746607723
1000 genomesrs746607723
hgdprs746607723
ensemblrs746607723
gopubmedrs746607723
geneviewrs746607723
scholarrs746607723
googlers746607723
pharmgkbrs746607723
gwascentralrs746607723
openSNPrs746607723
23andMers746607723
23andMe allrs746607723
SNP Nexus

SNPshotrs746607723
SNPdbers746607723
MSV3drs746607723
GWAS Ctlgrs746607723
Max Magnitude0
ClinVar
Risk rs746607723(A;A) rs746607723(C;C) rs746607723(T;T)
Alt rs746607723(A;A) rs746607723(C;C) rs746607723(T;T)
Reference Rs746607723(G;G)
Significance Pathogenic
Disease Non-immune hydrops fetalis Sialidosis
Variation info
Gene NEU1
CLNDBN Non-immune hydrops fetalis Sialidosis, type II
Reversed 0
HGVS NC_000006.11:g.31827574G>C
CLNSRC
CLNACC RCV000202594.1,