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rs79681911

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs79681911(A;A)
Make rs79681911(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position18269755
GeneSAA1
is asnp
is mentioned by
dbSNPrs79681911
ebirs79681911
HLIrs79681911
Exacrs79681911
Varsomers79681911
Maprs79681911
PheGenIrs79681911
hapmaprs79681911
1000 genomesrs79681911
hgdprs79681911
ensemblrs79681911
gopubmedrs79681911
geneviewrs79681911
scholarrs79681911
googlers79681911
pharmgkbrs79681911
gwascentralrs79681911
openSNPrs79681911
23andMers79681911
23andMe allrs79681911
SNP Nexus

SNPshotrs79681911
SNPdbers79681911
MSV3drs79681911
GWAS Ctlgrs79681911
GMAF0.006887
Max Magnitude0
OMIM104750
Desc
Variant0001
Relatedalso
ClinVar
Risk rs79681911(A;A)
Alt rs79681911(A;A)
Reference rs79681911(G;G)
Significance Pathogenic
Disease Serum amyloid a variant
Variation info
Gene SAA1
CLNDBN Serum amyloid a variant
Reversed 0
HGVS NC_000011.9:g.18291302G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000019735.27,