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rs229813

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs229813(C;T)
Make rs229813(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position83452020
is asnp
is mentioned by
dbSNPrs229813
ebirs229813
HLIrs229813
Exacrs229813
Varsomers229813
Maprs229813
PheGenIrs229813
hapmaprs229813
1000 genomesrs229813
hgdprs229813
ensemblrs229813
gopubmedrs229813
geneviewrs229813
scholarrs229813
googlers229813
pharmgkbrs229813
gwascentralrs229813
openSNPrs229813
23andMers229813
23andMe allrs229813
SNP Nexus

SNPshotrs229813
SNPdbers229813
MSV3drs229813
GWAS Ctlgrs229813
GMAF0.004591
Max Magnitude0
? (C;C) (C;T) (T;T) 28
OMIM606053
DescAUTISM, SUSCEPTIBILITY TO, 5; AUTS5
Variant
Relatedalso
OMIM603667
DescSOLUTE CARRIER FAMILY 25 (MITOCHONDRIAL CARRIER, ARALAR), MEMBER 12;
Variant
Relatedalso