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rs864309638

From SNPedia

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Geno Mag Summary
(A;A) 0 common in clinvar
Make rs864309638(A;C)
Make rs864309638(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position44124787
GeneEXT2
is asnp
is mentioned by
dbSNPrs864309638
ebirs864309638
HLIrs864309638
Exacrs864309638
Varsomers864309638
Maprs864309638
PheGenIrs864309638
hapmaprs864309638
1000 genomesrs864309638
hgdprs864309638
ensemblrs864309638
gopubmedrs864309638
geneviewrs864309638
scholarrs864309638
googlers864309638
pharmgkbrs864309638
gwascentralrs864309638
openSNPrs864309638
23andMers864309638
23andMe allrs864309638
SNP Nexus

SNPshotrs864309638
SNPdbers864309638
MSV3drs864309638
GWAS Ctlgrs864309638
Max Magnitude0
ClinVar
Risk rs864309638(C;C)
Alt rs864309638(C;C)
Reference rs864309638(A;A)
Significance Pathogenic
Disease Multiple exostoses type 2
Variation info
Gene EXT2
CLNDBN Multiple exostoses type 2
Reversed 0
HGVS NC_000011.9:g.44146337A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000002581.4,