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rs1057520608

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057520608(A;A)
Make rs1057520608(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position118110195
GeneEXT1
is asnp
is mentioned by
dbSNPrs1057520608
dbSNP (old)rs1057520608
ClinGenrs1057520608
ebirs1057520608
HLIrs1057520608
Exacrs1057520608
Gnomadrs1057520608
Varsomers1057520608
Maprs1057520608
PheGenIrs1057520608
Biobankrs1057520608
1000 genomesrs1057520608
hgdprs1057520608
ensemblrs1057520608
gopubmedrs1057520608
geneviewrs1057520608
scholarrs1057520608
googlers1057520608
pharmgkbrs1057520608
gwascentralrs1057520608
openSNPrs1057520608
23andMers1057520608
23andMe allrs1057520608
SNPshotrs1057520608
SNPdbers1057520608
MSV3drs1057520608
GWAS Ctlgrs1057520608
Max Magnitude0
ClinVar
Risk rs1057520608(A;A)
Alt rs1057520608(A;A)
Reference Rs1057520608(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene EXT1
CLNDBN not provided
Reversed 1
HGVS NC_000008.10:g.119122434A>T
CLNSRC
CLNACC RCV000440581.1,