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rs77743549

From SNPedia

Orientationplus
Make rs77743549(A;A)
Make rs77743549(A;C)
Make rs77743549(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position30752287
GeneINMT, INMT-FAM188B
is asnp
is mentioned by
dbSNPrs77743549
ebirs77743549
HLIrs77743549
Exacrs77743549
Varsomers77743549
Maprs77743549
PheGenIrs77743549
hapmaprs77743549
1000 genomesrs77743549
hgdprs77743549
ensemblrs77743549
gopubmedrs77743549
geneviewrs77743549
scholarrs77743549
googlers77743549
pharmgkbrs77743549
gwascentralrs77743549
openSNPrs77743549
23andMers77743549
23andMe allrs77743549
SNP Nexus

SNPshotrs77743549
SNPdbers77743549
MSV3drs77743549
GWAS Ctlgrs77743549
Max Magnitude

[PMID 26183064] Potential Association of INMT Nonsynonymous Variant (His46Pro) with Hirschsprung's Disease