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rs25925

From SNPedia

Orientationminus
Stabilizedminus
Make rs25925(C;C)
Make rs25925(C;G)
Make rs25925(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position111484055
is asnp
is mentioned by
dbSNPrs25925
ebirs25925
HLIrs25925
Exacrs25925
Varsomers25925
Maprs25925
PheGenIrs25925
hapmaprs25925
1000 genomesrs25925
hgdprs25925
ensemblrs25925
gopubmedrs25925
geneviewrs25925
scholarrs25925
googlers25925
pharmgkbrs25925
gwascentralrs25925
openSNPrs25925
23andMers25925
23andMe allrs25925
SNP Nexus

SNPshotrs25925
SNPdbers25925
MSV3drs25925
GWAS Ctlgrs25925
Max Magnitude
? (C;C) (C;G) (G;G) 28

[PMID 24442360] Common variants in genes of the postsynaptic FMRP signalling pathway are risk factors for autism spectrum disorders