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rs1057518140

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518140(C;T)
Make rs1057518140(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position103165911
GeneDYNC2H1
is asnp
is mentioned by
dbSNPrs1057518140
dbSNP (classic)rs1057518140
ClinGenrs1057518140
ebirs1057518140
HLIrs1057518140
Exacrs1057518140
Gnomadrs1057518140
Varsomers1057518140
LitVarrs1057518140
Maprs1057518140
PheGenIrs1057518140
Biobankrs1057518140
1000 genomesrs1057518140
hgdprs1057518140
ensemblrs1057518140
geneviewrs1057518140
scholarrs1057518140
googlers1057518140
pharmgkbrs1057518140
gwascentralrs1057518140
openSNPrs1057518140
23andMers1057518140
23andMe allrs1057518140
SNPshotrs1057518140
SNPdbers1057518140
MSV3drs1057518140
GWAS Ctlgrs1057518140
Max Magnitude0
ClinVar
Risk rs1057518140(T;T)
Alt rs1057518140(T;T)
Reference Rs1057518140(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,