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rs11099864

From SNPedia

Orientationplus
Stabilizedplus
Make rs11099864(A;A)
Make rs11099864(A;G)
Make rs11099864(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position152972202
GeneFHDC1
is asnp
is mentioned by
dbSNPrs11099864
ebirs11099864
HLIrs11099864
Exacrs11099864
Varsomers11099864
Maprs11099864
PheGenIrs11099864
hapmaprs11099864
1000 genomesrs11099864
hgdprs11099864
ensemblrs11099864
gopubmedrs11099864
geneviewrs11099864
scholarrs11099864
googlers11099864
pharmgkbrs11099864
gwascentralrs11099864
openSNPrs11099864
23andMers11099864
23andMe allrs11099864
SNP Nexus

SNPshotrs11099864
SNPdbers11099864
MSV3drs11099864
GWAS Ctlgrs11099864
GMAF0.4541
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 17362836]
Trait Amyotrophic lateral sclerosis
Title Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data
Risk Allele
P-val 0.0000090000000000000002
Odds Ratio 1.00 [0.80-1.40]


GET Evidence
rs11099864
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.484375
summary