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rs1085307731

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome1
Position161309897
is asnp
is mentioned by
dbSNPrs1085307731
dbSNP (old)rs1085307731
ClinGenrs1085307731
ebirs1085307731
HLIrs1085307731
Exacrs1085307731
Gnomadrs1085307731
Varsomers1085307731
Maprs1085307731
PheGenIrs1085307731
Biobankrs1085307731
1000 genomesrs1085307731
hgdprs1085307731
ensemblrs1085307731
gopubmedrs1085307731
geneviewrs1085307731
scholarrs1085307731
googlers1085307731
pharmgkbrs1085307731
gwascentralrs1085307731
openSNPrs1085307731
23andMers1085307731
23andMe allrs1085307731
SNPshotrs1085307731
SNPdbers1085307731
MSV3drs1085307731
GWAS Ctlgrs1085307731
Max Magnitude0
ClinVar
Risk rs1085307731(.;.)
Alt rs1085307731(.;.)
Reference Rs1085307731(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.161279688_161279718dup
CLNSRC
CLNACC RCV000490008.1,