Have questions? Visit https://www.reddit.com/r/SNPedia

rs745854387

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs745854387(C;T)
Make rs745854387(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position95104515
GeneBMPR1B
is asnp
is mentioned by
dbSNPrs745854387
ebirs745854387
HLIrs745854387
Exacrs745854387
Varsomers745854387
Maprs745854387
PheGenIrs745854387
hapmaprs745854387
1000 genomesrs745854387
hgdprs745854387
ensemblrs745854387
gopubmedrs745854387
geneviewrs745854387
scholarrs745854387
googlers745854387
pharmgkbrs745854387
gwascentralrs745854387
openSNPrs745854387
23andMers745854387
23andMe allrs745854387
SNP Nexus

SNPshotrs745854387
SNPdbers745854387
MSV3drs745854387
GWAS Ctlgrs745854387
Max Magnitude0
ClinVar
Risk rs745854387(T;T)
Alt rs745854387(T;T)
Reference rs745854387(C;C)
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.96025666C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000201128.2,