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rs150885084

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs150885084(A;A)
Make rs150885084(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome7
Position143330772
GeneCLCN1
is asnp
is mentioned by
dbSNPrs150885084
dbSNP (old)rs150885084
ClinGenrs150885084
ebirs150885084
HLIrs150885084
Exacrs150885084
Gnomadrs150885084
Varsomers150885084
Maprs150885084
PheGenIrs150885084
Biobankrs150885084
1000 genomesrs150885084
hgdprs150885084
ensemblrs150885084
gopubmedrs150885084
geneviewrs150885084
scholarrs150885084
googlers150885084
pharmgkbrs150885084
gwascentralrs150885084
openSNPrs150885084
23andMers150885084
23andMe allrs150885084
SNPshotrs150885084
SNPdbers150885084
MSV3drs150885084
GWAS Ctlgrs150885084
Max Magnitude0
ClinVar
Risk rs150885084(A;A)
Alt rs150885084(A;A)
Reference Rs150885084(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene CLCN1
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.143027865G>A
CLNSRC
CLNACC RCV000305463.1,