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rs864309636

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CTGT;CTGT) 0 common in clinvar
Make rs864309636(-;-)
Make rs864309636(-;CTGT)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position44108166
GeneEXT2
is asnp
is mentioned by
dbSNPrs864309636
dbSNP (old)rs864309636
ClinGenrs864309636
ebirs864309636
HLIrs864309636
Exacrs864309636
Gnomadrs864309636
Varsomers864309636
Maprs864309636
PheGenIrs864309636
Biobankrs864309636
1000 genomesrs864309636
hgdprs864309636
ensemblrs864309636
gopubmedrs864309636
geneviewrs864309636
scholarrs864309636
googlers864309636
pharmgkbrs864309636
gwascentralrs864309636
openSNPrs864309636
23andMers864309636
23andMe allrs864309636
SNP Nexus

SNPshotrs864309636
SNPdbers864309636
MSV3drs864309636
GWAS Ctlgrs864309636
Max Magnitude0
ClinVar
Risk rs864309636(-;-)
Alt rs864309636(-;-)
Reference Rs864309636(CTGT;CTGT)
Significance Pathogenic
Disease Multiple exostoses type 2
Variation info
Gene EXT2
CLNDBN Multiple exostoses type 2
Reversed 0
HGVS NC_000011.9:g.44129716_44129719delCTGT
CLNSRC OMIM Allelic Variant
CLNACC RCV000002575.2,