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rs1060502505

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060502505(C;T)
Make rs1060502505(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position38324807
GeneSPRED1
is asnp
is mentioned by
dbSNPrs1060502505
dbSNP (old)rs1060502505
ClinGenrs1060502505
ebirs1060502505
HLIrs1060502505
Exacrs1060502505
Gnomadrs1060502505
Varsomers1060502505
Maprs1060502505
PheGenIrs1060502505
Biobankrs1060502505
1000 genomesrs1060502505
hgdprs1060502505
ensemblrs1060502505
gopubmedrs1060502505
geneviewrs1060502505
scholarrs1060502505
googlers1060502505
pharmgkbrs1060502505
gwascentralrs1060502505
openSNPrs1060502505
23andMers1060502505
23andMe allrs1060502505
SNPshotrs1060502505
SNPdbers1060502505
MSV3drs1060502505
GWAS Ctlgrs1060502505
Max Magnitude0
ClinVar
Risk rs1060502505(T;T)
Alt rs1060502505(T;T)
Reference Rs1060502505(C;C)
Significance Pathogenic
Disease Legius syndrome
Variation info
Gene SPRED1
CLNDBN Legius syndrome
Reversed 0
HGVS NC_000015.9:g.38617008C>T
CLNSRC
CLNACC RCV000473065.1,