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rs775170915

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs775170915(-;-)
Make rs775170915(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position179551377
GeneAXDND1, NPHS2
is asnp
is mentioned by
dbSNPrs775170915
ebirs775170915
HLIrs775170915
Exacrs775170915
Varsomers775170915
Maprs775170915
PheGenIrs775170915
hapmaprs775170915
1000 genomesrs775170915
hgdprs775170915
ensemblrs775170915
gopubmedrs775170915
geneviewrs775170915
scholarrs775170915
googlers775170915
pharmgkbrs775170915
gwascentralrs775170915
openSNPrs775170915
23andMers775170915
23andMe allrs775170915
SNP Nexus

SNPshotrs775170915
SNPdbers775170915
MSV3drs775170915
GWAS Ctlgrs775170915
Max Magnitude0
ClinVar
Risk rs775170915(;)
Alt rs775170915(;)
Reference rs775170915(A;A)
Significance Probable-Pathogenic
Disease Nephrotic syndrome
Variation info
Gene NPHS2 AXDND1
CLNDBN Nephrotic syndrome, idiopathic, steroid-resistant
Reversed 0
HGVS NC_000001.10:g.179520512delA
CLNSRC Counsyl
CLNACC RCV000169369.1,