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Rs1051246

From SNPedia

Orientationminus
Stabilizedminus
Make rs1051246(C;C)
Make rs1051246(C;T)
Make rs1051246(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position79938062
GeneSFTPD
is asnp
is mentioned by
dbSNPrs1051246
ebirs1051246
Exacrs1051246
PheGenIrs1051246
nextbiors1051246
hapmaprs1051246
1000 genomesrs1051246
hgdprs1051246
ensemblrs1051246
gopubmedrs1051246
geneviewrs1051246
scholarrs1051246
googlers1051246
pharmgkbrs1051246
gwascentralrs1051246
openSNPrs1051246
23andMers1051246
23andMe allrs1051246
SNP Nexus

SNPshotrs1051246
SNPdbers1051246
MSV3drs1051246
GWAS Ctlgrs1051246
GMAF0.1469
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 21857919OA-icon.png] Evaluation of 15 functional candidate genes for association with chronic otitis media with effusion and/or recurrent otitis media (COME/ROM)


ClinVar
Risk rs1051246(C;C)
Alt rs1051246(C;C)
Reference rs1051246(T;T)
Significance Non-pathogenic
Disease not specified
Variation info
Gene SFTPD
CLNDBN not specified
Reversed 1
HGVS NC_000010.11:g.79938062A>G
CLNSRC
CLNACC RCV000155579.1,