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rs56211063

From SNPedia

Orientationplus
Stabilizedplus
Make rs56211063(C;C)
Make rs56211063(C;G)
Make rs56211063(G;G)
ReferenceGRCh38 38.1/142
Chromosome9
Position114823617
is asnp
is mentioned by
dbSNPrs56211063
ebirs56211063
HLIrs56211063
Exacrs56211063
Varsomers56211063
Maprs56211063
PheGenIrs56211063
hapmaprs56211063
1000 genomesrs56211063
hgdprs56211063
ensemblrs56211063
gopubmedrs56211063
geneviewrs56211063
scholarrs56211063
googlers56211063
pharmgkbrs56211063
gwascentralrs56211063
openSNPrs56211063
23andMers56211063
23andMe allrs56211063
SNP Nexus

SNPshotrs56211063
SNPdbers56211063
MSV3drs56211063
GWAS Ctlgrs56211063
Max Magnitude

[PMID 25899471] Human primary biliary cirrhosis-susceptible allele of rs4979462 enhances TNFSF15 expression by binding NF-1