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rs776315442

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs776315442(C;G)
Make rs776315442(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position103316576
GeneDYNC2H1
is asnp
is mentioned by
dbSNPrs776315442
ebirs776315442
HLIrs776315442
Exacrs776315442
Varsomers776315442
Maprs776315442
PheGenIrs776315442
hapmaprs776315442
1000 genomesrs776315442
hgdprs776315442
ensemblrs776315442
gopubmedrs776315442
geneviewrs776315442
scholarrs776315442
googlers776315442
pharmgkbrs776315442
gwascentralrs776315442
openSNPrs776315442
23andMers776315442
23andMe allrs776315442
SNP Nexus

SNPshotrs776315442
SNPdbers776315442
MSV3drs776315442
GWAS Ctlgrs776315442
Max Magnitude0
ClinVar
Risk rs776315442(G;G)
Alt rs776315442(G;G)
Reference rs776315442(C;C)
Significance Pathogenic
Disease Short-rib thoracic dysplasia 3 with or without polydactyly
Variation info
Gene DYNC2H1
CLNDBN Short-rib thoracic dysplasia 3 with or without polydactyly
Reversed 0
HGVS NC_000011.9:g.103187305C>G
CLNSRC
CLNACC RCV000180409.1,