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rs137853033

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137853033(A;G)
Make rs137853033(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position103163146
GeneDYNC2H1
is asnp
is mentioned by
dbSNPrs137853033
ebirs137853033
HLIrs137853033
Exacrs137853033
Varsomers137853033
Maprs137853033
PheGenIrs137853033
hapmaprs137853033
1000 genomesrs137853033
hgdprs137853033
ensemblrs137853033
gopubmedrs137853033
geneviewrs137853033
scholarrs137853033
googlers137853033
pharmgkbrs137853033
gwascentralrs137853033
openSNPrs137853033
23andMers137853033
23andMe allrs137853033
SNP Nexus

SNPshotrs137853033
SNPdbers137853033
MSV3drs137853033
GWAS Ctlgrs137853033
Max Magnitude0
OMIM603297
Desc
Variant0012
Relatedalso
ClinVar
Risk rs137853033(G;G)
Alt rs137853033(G;G)
Reference rs137853033(A;A)
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.103033875A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000006884.3,