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rs1060499775

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1060499775(-;A)
Make rs1060499775(A;A)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position55707550
GeneITGA7
is asnp
is mentioned by
dbSNPrs1060499775
dbSNP (old)rs1060499775
ClinGenrs1060499775
ebirs1060499775
HLIrs1060499775
Exacrs1060499775
Gnomadrs1060499775
Varsomers1060499775
Maprs1060499775
PheGenIrs1060499775
Biobankrs1060499775
1000 genomesrs1060499775
hgdprs1060499775
ensemblrs1060499775
gopubmedrs1060499775
geneviewrs1060499775
scholarrs1060499775
googlers1060499775
pharmgkbrs1060499775
gwascentralrs1060499775
openSNPrs1060499775
23andMers1060499775
23andMe allrs1060499775
SNPshotrs1060499775
SNPdbers1060499775
MSV3drs1060499775
GWAS Ctlgrs1060499775
Max Magnitude0
ClinVar
Risk rs1060499775(A;A)
Alt rs1060499775(A;A)
Reference Rs1060499775(-;-)
Significance Probable-Pathogenic
Disease Abnormality of brain morphology
Variation info
Gene ITGA7
CLNDBN Abnormality of brain morphology
Reversed 1
HGVS NC_000012.11:g.56101334_56101335insT
CLNSRC
CLNACC RCV000454351.1,