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

rs781712271

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs781712271(A;C)
Make rs781712271(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position162023387
GeneOLFML2B
is asnp
is mentioned by
dbSNPrs781712271
ebirs781712271
HLIrs781712271
Exacrs781712271
Varsomers781712271
Maprs781712271
PheGenIrs781712271
hapmaprs781712271
1000 genomesrs781712271
hgdprs781712271
ensemblrs781712271
gopubmedrs781712271
geneviewrs781712271
scholarrs781712271
googlers781712271
pharmgkbrs781712271
gwascentralrs781712271
openSNPrs781712271
23andMers781712271
23andMe allrs781712271
SNP Nexus

SNPshotrs781712271
SNPdbers781712271
MSV3drs781712271
GWAS Ctlgrs781712271
Max Magnitude0
ClinVar
Risk rs781712271(C;C)
Alt rs781712271(C;C)
Reference rs781712271(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene OLFML2B
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.161993177A>C
CLNSRC München/ Helmholtz Zentrum München
CLNACC RCV000201108.1,