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rs727503908

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727503908(G;T)
Make rs727503908(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position103220622
GeneDYNC2H1
is asnp
is mentioned by
dbSNPrs727503908
ebirs727503908
HLIrs727503908
Exacrs727503908
Varsomers727503908
Maprs727503908
PheGenIrs727503908
hapmaprs727503908
1000 genomesrs727503908
hgdprs727503908
ensemblrs727503908
gopubmedrs727503908
geneviewrs727503908
scholarrs727503908
googlers727503908
pharmgkbrs727503908
gwascentralrs727503908
openSNPrs727503908
23andMers727503908
23andMe allrs727503908
SNP Nexus

SNPshotrs727503908
SNPdbers727503908
MSV3drs727503908
GWAS Ctlgrs727503908
Max Magnitude0
ClinVar
Risk rs727503908(A,T;A,T)
Alt rs727503908(A,T;A,T)
Reference rs727503908(G;G)
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.103091351G>T
CLNSRC
CLNACC RCV000153172.3,