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rs76822696

From SNPedia

Merged intors62526245
Orientationplus
Make rs76822696(A;A)
Make rs76822696(A;C)
Make rs76822696(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome8
Position84016901
is asnp
is mentioned by
dbSNPrs76822696
ebirs76822696
HLIrs76822696
Exacrs76822696
Varsomers76822696
Maprs76822696
PheGenIrs76822696
hapmaprs76822696
1000 genomesrs76822696
hgdprs76822696
ensemblrs76822696
gopubmedrs76822696
geneviewrs76822696
scholarrs76822696
googlers76822696
pharmgkbrs76822696
gwascentralrs76822696
openSNPrs76822696
23andMers76822696
23andMe allrs76822696
SNP Nexus

SNPshotrs76822696
SNPdbers76822696
MSV3drs76822696
GWAS Ctlgrs76822696
StatusMerged into rs62526245
Max Magnitude

[PMID 26507551] Genome-wide association study identifies African-ancestry specific variants for metabolic syndrome