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rs1059046

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1059046(A;A)
Make rs1059046(A;C)
ReferenceGRCh38 38.1/142
Chromosome10
Position79559458
GeneSFTPA2
is asnp
is mentioned by
dbSNPrs1059046
ebirs1059046
HLIrs1059046
Exacrs1059046
Varsomers1059046
Maprs1059046
PheGenIrs1059046
hapmaprs1059046
1000 genomesrs1059046
hgdprs1059046
ensemblrs1059046
gopubmedrs1059046
geneviewrs1059046
scholarrs1059046
googlers1059046
pharmgkbrs1059046
gwascentralrs1059046
openSNPrs1059046
23andMers1059046
23andMe allrs1059046
SNP Nexus

SNPshotrs1059046
SNPdbers1059046
MSV3drs1059046
GWAS Ctlgrs1059046
Max Magnitude0

[PMID 24950659OA-icon.png] Surfactant protein A genetic variants associate with severe respiratory insufficiency in pandemic influenza A virus infection

ClinVar
Risk rs1059046(A,G;A,G)
Alt rs1059046(A,G;A,G)
Reference rs1059046(C;C)
Significance Non-pathogenic
Disease not specified
Variation info
Gene SFTPA2
CLNDBN not specified
Reversed 1
HGVS NC_000010.10:g.81319214G>T
CLNSRC
CLNACC RCV000221077.1,