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

rs150855173

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs150855173(A;A)
Make rs150855173(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position35831092
GeneNPHS1
is asnp
is mentioned by
dbSNPrs150855173
ebirs150855173
HLIrs150855173
Exacrs150855173
Varsomers150855173
Maprs150855173
PheGenIrs150855173
hapmaprs150855173
1000 genomesrs150855173
hgdprs150855173
ensemblrs150855173
gopubmedrs150855173
geneviewrs150855173
scholarrs150855173
googlers150855173
pharmgkbrs150855173
gwascentralrs150855173
openSNPrs150855173
23andMers150855173
23andMe allrs150855173
SNP Nexus

SNPshotrs150855173
SNPdbers150855173
MSV3drs150855173
GWAS Ctlgrs150855173
Max Magnitude0
ClinVar
Risk rs150855173(A;A)
Alt rs150855173(A;A)
Reference rs150855173(G;G)
Significance Probable-Pathogenic
Disease Finnish congenital nephrotic syndrome
Variation info
Gene NPHS1
CLNDBN Finnish congenital nephrotic syndrome
Reversed 0
HGVS NC_000019.9:g.36321994G>A
CLNSRC
CLNACC RCV000169477.1,