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rs7721142

From SNPedia

Orientationplus
Stabilizedplus
Make rs7721142(C;C)
Make rs7721142(C;G)
Make rs7721142(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position157525400
GeneADAM19
is asnp
is mentioned by
dbSNPrs7721142
ebirs7721142
HLIrs7721142
Exacrs7721142
Varsomers7721142
Maprs7721142
PheGenIrs7721142
hapmaprs7721142
1000 genomesrs7721142
hgdprs7721142
ensemblrs7721142
gopubmedrs7721142
geneviewrs7721142
scholarrs7721142
googlers7721142
pharmgkbrs7721142
gwascentralrs7721142
openSNPrs7721142
23andMers7721142
23andMe allrs7721142
SNP Nexus

SNPshotrs7721142
SNPdbers7721142
MSV3drs7721142
GWAS Ctlgrs7721142
GMAF0.2998
Max Magnitude
? (C;C) (C;G) (G;G) 28

[PMID 19319892] A narrow and highly significant linkage signal for severe bipolar disorder in the chromosome 5q33 region in Latin American pedigrees.