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

rs786205518

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205518(A;C)
Make rs786205518(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome19
Position35831298
GeneNPHS1
is asnp
is mentioned by
dbSNPrs786205518
ebirs786205518
HLIrs786205518
Exacrs786205518
Varsomers786205518
Maprs786205518
PheGenIrs786205518
hapmaprs786205518
1000 genomesrs786205518
hgdprs786205518
ensemblrs786205518
gopubmedrs786205518
geneviewrs786205518
scholarrs786205518
googlers786205518
pharmgkbrs786205518
gwascentralrs786205518
openSNPrs786205518
23andMers786205518
23andMe allrs786205518
SNP Nexus

SNPshotrs786205518
SNPdbers786205518
MSV3drs786205518
GWAS Ctlgrs786205518
Max Magnitude0
ClinVar
Risk rs786205518(C;C)
Alt rs786205518(C;C)
Reference rs786205518(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NPHS1
CLNDBN not provided
Reversed 1
HGVS NC_000019.9:g.36322200T>G
CLNSRC
CLNACC RCV000171282.1,