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rs1057521132

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057521132(G;T)
Make rs1057521132(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position44109284
GeneEXT2
is asnp
is mentioned by
dbSNPrs1057521132
dbSNP (old)rs1057521132
ClinGenrs1057521132
ebirs1057521132
HLIrs1057521132
Exacrs1057521132
Gnomadrs1057521132
Varsomers1057521132
Maprs1057521132
PheGenIrs1057521132
Biobankrs1057521132
1000 genomesrs1057521132
hgdprs1057521132
ensemblrs1057521132
gopubmedrs1057521132
geneviewrs1057521132
scholarrs1057521132
googlers1057521132
pharmgkbrs1057521132
gwascentralrs1057521132
openSNPrs1057521132
23andMers1057521132
23andMe allrs1057521132
SNPshotrs1057521132
SNPdbers1057521132
MSV3drs1057521132
GWAS Ctlgrs1057521132
Max Magnitude0
ClinVar
Risk rs1057521132(T;T)
Alt rs1057521132(T;T)
Reference Rs1057521132(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene EXT2
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.44130834G>T
CLNSRC
CLNACC RCV000443576.1,