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rs121964995

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121964995(C;C)
Make rs121964995(C;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position100264835
GeneINVS
is asnp
is mentioned by
dbSNPrs121964995
ebirs121964995
HLIrs121964995
Exacrs121964995
Varsomers121964995
Maprs121964995
PheGenIrs121964995
hapmaprs121964995
1000 genomesrs121964995
hgdprs121964995
ensemblrs121964995
gopubmedrs121964995
geneviewrs121964995
scholarrs121964995
googlers121964995
pharmgkbrs121964995
gwascentralrs121964995
openSNPrs121964995
23andMers121964995
23andMe allrs121964995
SNP Nexus

SNPshotrs121964995
SNPdbers121964995
MSV3drs121964995
GWAS Ctlgrs121964995
Max Magnitude0
OMIM243305
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121964995(C;C)
Alt rs121964995(C;C)
Reference rs121964995(T;T)
Significance Pathogenic
Disease Infantile nephronophthisis
Variation info
Gene INVS
CLNDBN Infantile nephronophthisis
Reversed 0
HGVS NC_000009.11:g.103027117T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000012738.22,