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rs1057520737

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520737(C;T)
Make rs1057520737(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position68192949
GeneOPHN1
is asnp
is mentioned by
dbSNPrs1057520737
dbSNP (old)rs1057520737
ClinGenrs1057520737
ebirs1057520737
HLIrs1057520737
Exacrs1057520737
Gnomadrs1057520737
Varsomers1057520737
Maprs1057520737
PheGenIrs1057520737
Biobankrs1057520737
1000 genomesrs1057520737
hgdprs1057520737
ensemblrs1057520737
gopubmedrs1057520737
geneviewrs1057520737
scholarrs1057520737
googlers1057520737
pharmgkbrs1057520737
gwascentralrs1057520737
openSNPrs1057520737
23andMers1057520737
23andMe allrs1057520737
SNPshotrs1057520737
SNPdbers1057520737
MSV3drs1057520737
GWAS Ctlgrs1057520737
Max Magnitude0
ClinVar
Risk rs1057520737(T;T)
Alt rs1057520737(T;T)
Reference Rs1057520737(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene OPHN1
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.67412791G>A
CLNSRC
CLNACC RCV000429803.1,