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rs1057518083

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518083(C;T)
Make rs1057518083(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome14
Position101986552
GeneDYNC1H1
is asnp
is mentioned by
dbSNPrs1057518083
dbSNP (classic)rs1057518083
ClinGenrs1057518083
ebirs1057518083
HLIrs1057518083
Exacrs1057518083
Gnomadrs1057518083
Varsomers1057518083
LitVarrs1057518083
Maprs1057518083
PheGenIrs1057518083
Biobankrs1057518083
1000 genomesrs1057518083
hgdprs1057518083
ensemblrs1057518083
geneviewrs1057518083
scholarrs1057518083
googlers1057518083
pharmgkbrs1057518083
gwascentralrs1057518083
openSNPrs1057518083
23andMers1057518083
23andMe allrs1057518083
SNPshotrs1057518083
SNPdbers1057518083
MSV3drs1057518083
GWAS Ctlgrs1057518083
Max Magnitude0
ClinVar
Risk rs1057518083(T;T)
Alt rs1057518083(T;T)
Reference Rs1057518083(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene DYNC1H1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.102452889C>T
CLNSRC
CLNACC RCV000413532.1,