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rs607755

From SNPedia

Orientationplus
Stabilizedplus
Make rs607755(A;A)
Make rs607755(A;G)
Make rs607755(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position103749507
GeneRELN
is asnp
is mentioned by
dbSNPrs607755
ebirs607755
HLIrs607755
Exacrs607755
Varsomers607755
Maprs607755
PheGenIrs607755
hapmaprs607755
1000 genomesrs607755
hgdprs607755
ensemblrs607755
gopubmedrs607755
geneviewrs607755
scholarrs607755
googlers607755
pharmgkbrs607755
gwascentralrs607755
openSNPrs607755
23andMers607755
23andMe allrs607755
SNP Nexus

SNPshotrs607755
SNPdbers607755
MSV3drs607755
GWAS Ctlgrs607755
GMAF0.4651
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 18599960] rs607755 and rs2229874 appear to relate to females and Alzheimer's disease


ClinVar
Risk rs607755(G;G)
Alt rs607755(G;G)
Reference rs607755(A;A)
Significance Other
Disease not specified
Variation info
Gene RELN
CLNDBN not specified
Reversed 0
HGVS NC_000007.13:g.103389954A>G
CLNSRC ClinVar University of Chicago
CLNACC RCV000081236.7,