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rs376879175

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs376879175(C;T)
Make rs376879175(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position100293039
GeneINVS
is asnp
is mentioned by
dbSNPrs376879175
ebirs376879175
HLIrs376879175
Exacrs376879175
Varsomers376879175
Maprs376879175
PheGenIrs376879175
hapmaprs376879175
1000 genomesrs376879175
hgdprs376879175
ensemblrs376879175
gopubmedrs376879175
geneviewrs376879175
scholarrs376879175
googlers376879175
pharmgkbrs376879175
gwascentralrs376879175
openSNPrs376879175
23andMers376879175
23andMe allrs376879175
SNP Nexus

SNPshotrs376879175
SNPdbers376879175
MSV3drs376879175
GWAS Ctlgrs376879175
Max Magnitude0
ClinVar
Risk rs376879175(A,T;A,T)
Alt rs376879175(A,T;A,T)
Reference rs376879175(C;C)
Significance Pathogenic
Disease Nephronophthisis
Variation info
Gene INVS
CLNDBN Nephronophthisis
Reversed 0
HGVS NC_000009.11:g.103055321C>T
CLNSRC
CLNACC RCV000234833.1,