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rs1085308000

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome15
Position92978253
GeneCHD2
is asnp
is mentioned by
dbSNPrs1085308000
dbSNP (old)rs1085308000
ClinGenrs1085308000
ebirs1085308000
HLIrs1085308000
Exacrs1085308000
Gnomadrs1085308000
Varsomers1085308000
Maprs1085308000
PheGenIrs1085308000
Biobankrs1085308000
1000 genomesrs1085308000
hgdprs1085308000
ensemblrs1085308000
gopubmedrs1085308000
geneviewrs1085308000
scholarrs1085308000
googlers1085308000
pharmgkbrs1085308000
gwascentralrs1085308000
openSNPrs1085308000
23andMers1085308000
23andMe allrs1085308000
SNPshotrs1085308000
SNPdbers1085308000
MSV3drs1085308000
GWAS Ctlgrs1085308000
Max Magnitude0
ClinVar
Risk rs1085308000(T;T)
Alt rs1085308000(T;T)
Reference Rs1085308000(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CHD2
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.93521483C>T
CLNSRC
CLNACC RCV000489893.1,