Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057518108

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518108(C;C)
Make rs1057518108(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position103515385
GeneRELN
is asnp
is mentioned by
dbSNPrs1057518108
dbSNP (old)rs1057518108
ClinGenrs1057518108
ebirs1057518108
HLIrs1057518108
Exacrs1057518108
Gnomadrs1057518108
Varsomers1057518108
Maprs1057518108
PheGenIrs1057518108
Biobankrs1057518108
1000 genomesrs1057518108
hgdprs1057518108
ensemblrs1057518108
gopubmedrs1057518108
geneviewrs1057518108
scholarrs1057518108
googlers1057518108
pharmgkbrs1057518108
gwascentralrs1057518108
openSNPrs1057518108
23andMers1057518108
23andMe allrs1057518108
SNPshotrs1057518108
SNPdbers1057518108
MSV3drs1057518108
GWAS Ctlgrs1057518108
Max Magnitude0
ClinVar
Risk rs1057518108(C;C)
Alt rs1057518108(C;C)
Reference Rs1057518108(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RELN
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.103155832C>G
CLNSRC
CLNACC RCV000414213.1,