Have questions? Visit https://www.reddit.com/r/SNPedia

rs757725348

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs757725348(A;A)
Make rs757725348(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome14
Position102033982
GeneDYNC1H1
is asnp
is mentioned by
dbSNPrs757725348
ebirs757725348
HLIrs757725348
Exacrs757725348
Varsomers757725348
Maprs757725348
PheGenIrs757725348
hapmaprs757725348
1000 genomesrs757725348
hgdprs757725348
ensemblrs757725348
gopubmedrs757725348
geneviewrs757725348
scholarrs757725348
googlers757725348
pharmgkbrs757725348
gwascentralrs757725348
openSNPrs757725348
23andMers757725348
23andMe allrs757725348
SNP Nexus

SNPshotrs757725348
SNPdbers757725348
MSV3drs757725348
GWAS Ctlgrs757725348
Max Magnitude0
ClinVar
Risk rs757725348(A;A)
Alt rs757725348(A;A)
Reference rs757725348(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene DYNC1H1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.102500319C>T
CLNSRC
CLNACC RCV000235908.1,