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rs201850090

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs201850090(C;T)
Make rs201850090(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position143342009
GeneCLCN1
is asnp
is mentioned by
dbSNPrs201850090
dbSNP (old)rs201850090
ClinGenrs201850090
ebirs201850090
HLIrs201850090
Exacrs201850090
Gnomadrs201850090
Varsomers201850090
Maprs201850090
PheGenIrs201850090
Biobankrs201850090
1000 genomesrs201850090
hgdprs201850090
ensemblrs201850090
gopubmedrs201850090
geneviewrs201850090
scholarrs201850090
googlers201850090
pharmgkbrs201850090
gwascentralrs201850090
openSNPrs201850090
23andMers201850090
23andMe allrs201850090
SNPshotrs201850090
SNPdbers201850090
MSV3drs201850090
GWAS Ctlgrs201850090
Max Magnitude0
ClinVar
Risk rs201850090(T;T)
Alt rs201850090(T;T)
Reference Rs201850090(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CLCN1
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.143039102C>T
CLNSRC
CLNACC RCV000437007.1,