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rs150038620

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs150038620(C;T)
Make rs150038620(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position35842551
GeneNPHS1
is asnp
is mentioned by
dbSNPrs150038620
ebirs150038620
HLIrs150038620
Exacrs150038620
Varsomers150038620
Maprs150038620
PheGenIrs150038620
hapmaprs150038620
1000 genomesrs150038620
hgdprs150038620
ensemblrs150038620
gopubmedrs150038620
geneviewrs150038620
scholarrs150038620
googlers150038620
pharmgkbrs150038620
gwascentralrs150038620
openSNPrs150038620
23andMers150038620
23andMe allrs150038620
SNP Nexus

SNPshotrs150038620
SNPdbers150038620
MSV3drs150038620
GWAS Ctlgrs150038620
Max Magnitude0
ClinVar
Risk rs150038620(T;T)
Alt rs150038620(T;T)
Reference rs150038620(C;C)
Significance Probable-Pathogenic
Disease Finnish congenital nephrotic syndrome
Variation info
Gene NPHS1
CLNDBN Finnish congenital nephrotic syndrome
Reversed 0
HGVS NC_000019.9:g.36333453C>T
CLNSRC
CLNACC RCV000169038.1,