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

rs869025613

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869025613(A;A)
Make rs869025613(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome4
Position95124982
GeneBMPR1B
is asnp
is mentioned by
dbSNPrs869025613
ebirs869025613
HLIrs869025613
Exacrs869025613
Varsomers869025613
Maprs869025613
PheGenIrs869025613
hapmaprs869025613
1000 genomesrs869025613
hgdprs869025613
ensemblrs869025613
gopubmedrs869025613
geneviewrs869025613
scholarrs869025613
googlers869025613
pharmgkbrs869025613
gwascentralrs869025613
openSNPrs869025613
23andMers869025613
23andMe allrs869025613
SNP Nexus

SNPshotrs869025613
SNPdbers869025613
MSV3drs869025613
GWAS Ctlgrs869025613
Max Magnitude0
ClinVar
Risk rs869025613(A;A)
Alt rs869025613(A;A)
Reference rs869025613(G;G)
Significance Pathogenic
Disease Brachydactyly
Variation info
Gene BMPR1B
CLNDBN Brachydactyly, type a1, d
Reversed 0
HGVS NC_000004.11:g.96046133G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000208781.1,