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rs1057518250

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518250(C;G)
Make rs1057518250(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome14
Position101986094
GeneDYNC1H1
is asnp
is mentioned by
dbSNPrs1057518250
dbSNP (old)rs1057518250
ClinGenrs1057518250
ebirs1057518250
HLIrs1057518250
Exacrs1057518250
Gnomadrs1057518250
Varsomers1057518250
Maprs1057518250
PheGenIrs1057518250
Biobankrs1057518250
1000 genomesrs1057518250
hgdprs1057518250
ensemblrs1057518250
gopubmedrs1057518250
geneviewrs1057518250
scholarrs1057518250
googlers1057518250
pharmgkbrs1057518250
gwascentralrs1057518250
openSNPrs1057518250
23andMers1057518250
23andMe allrs1057518250
SNPshotrs1057518250
SNPdbers1057518250
MSV3drs1057518250
GWAS Ctlgrs1057518250
Max Magnitude0
ClinVar
Risk rs1057518250(G;G)
Alt rs1057518250(G;G)
Reference Rs1057518250(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DYNC1H1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.102452431C>G
CLNSRC
CLNACC RCV000413767.1,