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rs786205657

From SNPedia

Orientationminus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs786205657(-;-)
Make rs786205657(-;AT)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position103539227
GeneLOC105375435, RELN
is asnp
is mentioned by
dbSNPrs786205657
ebirs786205657
HLIrs786205657
Exacrs786205657
Varsomers786205657
Maprs786205657
PheGenIrs786205657
hapmaprs786205657
1000 genomesrs786205657
hgdprs786205657
ensemblrs786205657
gopubmedrs786205657
geneviewrs786205657
scholarrs786205657
googlers786205657
pharmgkbrs786205657
gwascentralrs786205657
openSNPrs786205657
23andMers786205657
23andMe allrs786205657
SNP Nexus

SNPshotrs786205657
SNPdbers786205657
MSV3drs786205657
GWAS Ctlgrs786205657
Max Magnitude0
ClinVar
Risk rs786205657(;)
Alt rs786205657(;)
Reference rs786205657(AT;AT)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RELN
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.103179674_103179675delAT
CLNSRC
CLNACC RCV000171531.1,