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rs863225042

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863225042(A;A)
Make rs863225042(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position95129933
GeneBMPR1B
is asnp
is mentioned by
dbSNPrs863225042
ebirs863225042
HLIrs863225042
Exacrs863225042
Varsomers863225042
Maprs863225042
PheGenIrs863225042
hapmaprs863225042
1000 genomesrs863225042
hgdprs863225042
ensemblrs863225042
gopubmedrs863225042
geneviewrs863225042
scholarrs863225042
googlers863225042
pharmgkbrs863225042
gwascentralrs863225042
openSNPrs863225042
23andMers863225042
23andMe allrs863225042
SNP Nexus

SNPshotrs863225042
SNPdbers863225042
MSV3drs863225042
GWAS Ctlgrs863225042
Max Magnitude0
ClinVar
Risk rs863225042(A;A)
Alt rs863225042(A;A)
Reference rs863225042(G;G)
Significance Pathogenic
Disease Chondrodysplasia acromesomelic with genital anomalies
Variation info
Gene BMPR1B
CLNDBN Chondrodysplasia acromesomelic with genital anomalies
Reversed 0
HGVS NC_000004.11:g.96051084G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000201044.2,