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rs1057518287

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518287(A;A)
Make rs1057518287(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome14
Position102008245
GeneDYNC1H1
is asnp
is mentioned by
dbSNPrs1057518287
dbSNP (old)rs1057518287
ClinGenrs1057518287
ebirs1057518287
HLIrs1057518287
Exacrs1057518287
Gnomadrs1057518287
Varsomers1057518287
Maprs1057518287
PheGenIrs1057518287
Biobankrs1057518287
1000 genomesrs1057518287
hgdprs1057518287
ensemblrs1057518287
gopubmedrs1057518287
geneviewrs1057518287
scholarrs1057518287
googlers1057518287
pharmgkbrs1057518287
gwascentralrs1057518287
openSNPrs1057518287
23andMers1057518287
23andMe allrs1057518287
SNPshotrs1057518287
SNPdbers1057518287
MSV3drs1057518287
GWAS Ctlgrs1057518287
Max Magnitude0
ClinVar
Risk rs1057518287(A;A)
Alt rs1057518287(A;A)
Reference Rs1057518287(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DYNC1H1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.102474582G>A
CLNSRC
CLNACC RCV000414412.1,