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rs1085307938

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome3
Position184359124
GeneCLCN2
is asnp
is mentioned by
dbSNPrs1085307938
dbSNP (old)rs1085307938
ClinGenrs1085307938
ebirs1085307938
HLIrs1085307938
Exacrs1085307938
Gnomadrs1085307938
Varsomers1085307938
LitVarrs1085307938
Maprs1085307938
PheGenIrs1085307938
Biobankrs1085307938
1000 genomesrs1085307938
hgdprs1085307938
ensemblrs1085307938
gopubmedrs1085307938
geneviewrs1085307938
scholarrs1085307938
googlers1085307938
pharmgkbrs1085307938
gwascentralrs1085307938
openSNPrs1085307938
23andMers1085307938
23andMe allrs1085307938
SNPshotrs1085307938
SNPdbers1085307938
MSV3drs1085307938
GWAS Ctlgrs1085307938
Max Magnitude0
ClinVar
Risk rs1085307938(A;A)
Alt rs1085307938(A;A)
Reference Rs1085307938(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CLCN2
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.184076912C>T
CLNSRC
CLNACC RCV000489700.1,