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rs1057523839

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057523839(A;A)
Make rs1057523839(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome14
Position101985927
GeneDYNC1H1
is asnp
is mentioned by
dbSNPrs1057523839
dbSNP (old)rs1057523839
ClinGenrs1057523839
ebirs1057523839
HLIrs1057523839
Exacrs1057523839
Gnomadrs1057523839
Varsomers1057523839
LitVarrs1057523839
Maprs1057523839
PheGenIrs1057523839
Biobankrs1057523839
1000 genomesrs1057523839
hgdprs1057523839
ensemblrs1057523839
gopubmedrs1057523839
geneviewrs1057523839
scholarrs1057523839
googlers1057523839
pharmgkbrs1057523839
gwascentralrs1057523839
openSNPrs1057523839
23andMers1057523839
23andMe allrs1057523839
SNPshotrs1057523839
SNPdbers1057523839
MSV3drs1057523839
GWAS Ctlgrs1057523839
Max Magnitude0
ClinVar
Risk rs1057523839(A;A)
Alt rs1057523839(A;A)
Reference Rs1057523839(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DYNC1H1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.102452264C>A
CLNSRC
CLNACC RCV000435368.1,