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rs1057517814

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517814(A;A)
Make rs1057517814(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position103522084
GeneRELN
is asnp
is mentioned by
dbSNPrs1057517814
dbSNP (old)rs1057517814
ClinGenrs1057517814
ebirs1057517814
HLIrs1057517814
Exacrs1057517814
Gnomadrs1057517814
Varsomers1057517814
Maprs1057517814
PheGenIrs1057517814
Biobankrs1057517814
1000 genomesrs1057517814
hgdprs1057517814
ensemblrs1057517814
gopubmedrs1057517814
geneviewrs1057517814
scholarrs1057517814
googlers1057517814
pharmgkbrs1057517814
gwascentralrs1057517814
openSNPrs1057517814
23andMers1057517814
23andMe allrs1057517814
SNPshotrs1057517814
SNPdbers1057517814
MSV3drs1057517814
GWAS Ctlgrs1057517814
Max Magnitude0
ClinVar
Risk rs1057517814(A;A)
Alt rs1057517814(A;A)
Reference Rs1057517814(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RELN
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.103162531C>T
CLNSRC
CLNACC RCV000413697.1,