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rs137853892

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137853892(C;C)
Make rs137853892(C;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position75566582
GeneSERPINH1
is asnp
is mentioned by
dbSNPrs137853892
ebirs137853892
HLIrs137853892
Exacrs137853892
Varsomers137853892
Maprs137853892
PheGenIrs137853892
hapmaprs137853892
1000 genomesrs137853892
hgdprs137853892
ensemblrs137853892
gopubmedrs137853892
geneviewrs137853892
scholarrs137853892
googlers137853892
pharmgkbrs137853892
gwascentralrs137853892
openSNPrs137853892
23andMers137853892
23andMe allrs137853892
SNP Nexus

SNPshotrs137853892
SNPdbers137853892
MSV3drs137853892
GWAS Ctlgrs137853892
Max Magnitude0
ClinVar
Risk rs137853892(C;C)
Alt rs137853892(C;C)
Reference rs137853892(T;T)
Significance Pathogenic
Disease Osteogenesis imperfecta type 10
Variation info
Gene SERPINH1
CLNDBN Osteogenesis imperfecta type 10
Reversed 0
HGVS NC_000011.9:g.75277627T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000023052.4,