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rs797045915

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797045915(C;T)
Make rs797045915(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position103557992
GeneRELN
is asnp
is mentioned by
dbSNPrs797045915
ebirs797045915
HLIrs797045915
Exacrs797045915
Varsomers797045915
Maprs797045915
PheGenIrs797045915
hapmaprs797045915
1000 genomesrs797045915
hgdprs797045915
ensemblrs797045915
gopubmedrs797045915
geneviewrs797045915
scholarrs797045915
googlers797045915
pharmgkbrs797045915
gwascentralrs797045915
openSNPrs797045915
23andMers797045915
23andMe allrs797045915
SNP Nexus

SNPshotrs797045915
SNPdbers797045915
MSV3drs797045915
GWAS Ctlgrs797045915
Max Magnitude0
ClinVar
Risk rs797045915(T;T)
Alt rs797045915(T;T)
Reference rs797045915(C;C)
Significance Pathogenic
Disease Lissencephaly 2 (Norman-Roberts type)
Variation info
Gene RELN
CLNDBN Lissencephaly 2 (Norman-Roberts type)
Reversed 1
HGVS NC_000007.13:g.103198439G>A
CLNSRC
CLNACC RCV000194711.1,