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rs11986414

From SNPedia

Orientationplus
Stabilizedplus
Make rs11986414(A;A)
Make rs11986414(A;G)
Make rs11986414(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position1798784
is asnp
is mentioned by
dbSNPrs11986414
ebirs11986414
HLIrs11986414
Exacrs11986414
Varsomers11986414
Maprs11986414
PheGenIrs11986414
hapmaprs11986414
1000 genomesrs11986414
hgdprs11986414
ensemblrs11986414
gopubmedrs11986414
geneviewrs11986414
scholarrs11986414
googlers11986414
pharmgkbrs11986414
gwascentralrs11986414
openSNPrs11986414
23andMers11986414
23andMe allrs11986414
SNP Nexus

SNPshotrs11986414
SNPdbers11986414
MSV3drs11986414
GWAS Ctlgrs11986414
GMAF0.2677
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 22388998OA-icon.png] Genome-wide association study of N370S homozygous Gaucher disease reveals the candidacy of CLN8 gene as a genetic modifier contributing to extreme phenotypic variation