Have questions? Visit https://www.reddit.com/r/SNPedia

rs769345284

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs769345284(A;A)
Make rs769345284(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position151537898
GeneNEB
is asnp
is mentioned by
dbSNPrs769345284
ebirs769345284
HLIrs769345284
Exacrs769345284
Varsomers769345284
Maprs769345284
PheGenIrs769345284
hapmaprs769345284
1000 genomesrs769345284
hgdprs769345284
ensemblrs769345284
gopubmedrs769345284
geneviewrs769345284
scholarrs769345284
googlers769345284
pharmgkbrs769345284
gwascentralrs769345284
openSNPrs769345284
23andMers769345284
23andMe allrs769345284
SNP Nexus

SNPshotrs769345284
SNPdbers769345284
MSV3drs769345284
GWAS Ctlgrs769345284
Max Magnitude0
ClinVar
Risk rs769345284(A;A)
Alt rs769345284(A;A)
Reference rs769345284(G;G)
Significance Probable-Pathogenic
Disease Non-immune hydrops fetalis
Variation info
Gene NEB
CLNDBN Non-immune hydrops fetalis
Reversed 0
HGVS NC_000002.11:g.152394412G>A
CLNSRC
CLNACC RCV000170577.1,