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

rs864309637

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs864309637(A;A)
Make rs864309637(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position44171743
GeneEXT2
is asnp
is mentioned by
dbSNPrs864309637
ebirs864309637
HLIrs864309637
Exacrs864309637
Varsomers864309637
Maprs864309637
PheGenIrs864309637
hapmaprs864309637
1000 genomesrs864309637
hgdprs864309637
ensemblrs864309637
gopubmedrs864309637
geneviewrs864309637
scholarrs864309637
googlers864309637
pharmgkbrs864309637
gwascentralrs864309637
openSNPrs864309637
23andMers864309637
23andMe allrs864309637
SNP Nexus

SNPshotrs864309637
SNPdbers864309637
MSV3drs864309637
GWAS Ctlgrs864309637
Max Magnitude0
ClinVar
Risk rs864309637(A;A)
Alt rs864309637(A;A)
Reference rs864309637(G;G)
Significance Pathogenic
Disease Multiple exostoses type 2
Variation info
Gene EXT2
CLNDBN Multiple exostoses type 2
Reversed 0
HGVS NC_000011.9:g.44193293G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000002577.2,