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rs1043384862

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position103165911
GeneDYNC2H1
is asnp
is mentioned by
dbSNPrs1043384862
dbSNP (old)rs1043384862
ClinGenrs1043384862
ebirs1043384862
HLIrs1043384862
Exacrs1043384862
Gnomadrs1043384862
Varsomers1043384862
LitVarrs1043384862
Maprs1043384862
PheGenIrs1043384862
Biobankrs1043384862
1000 genomesrs1043384862
hgdprs1043384862
ensemblrs1043384862
gopubmedrs1043384862
geneviewrs1043384862
scholarrs1043384862
googlers1043384862
pharmgkbrs1043384862
gwascentralrs1043384862
openSNPrs1043384862
23andMers1043384862
23andMe allrs1043384862
SNPshotrs1043384862
SNPdbers1043384862
MSV3drs1043384862
GWAS Ctlgrs1043384862
Max Magnitude0
ClinVar
Risk rs1043384862(T;T)
Alt rs1043384862(T;T)
Reference Rs1043384862(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DYNC2H1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.103036640C>T
CLNSRC
CLNACC RCV000413597.1,