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rs121917738

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121917738(C;C)
Make rs121917738(C;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position79557363
GeneSFTPA2
is asnp
is mentioned by
dbSNPrs121917738
ebirs121917738
HLIrs121917738
Exacrs121917738
Varsomers121917738
Maprs121917738
PheGenIrs121917738
hapmaprs121917738
1000 genomesrs121917738
hgdprs121917738
ensemblrs121917738
gopubmedrs121917738
geneviewrs121917738
scholarrs121917738
googlers121917738
pharmgkbrs121917738
gwascentralrs121917738
openSNPrs121917738
23andMers121917738
23andMe allrs121917738
SNP Nexus

SNPshotrs121917738
SNPdbers121917738
MSV3drs121917738
GWAS Ctlgrs121917738
Max Magnitude0
OMIM178642
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121917738(C;C)
Alt rs121917738(C;C)
Reference rs121917738(T;T)
Significance Pathogenic
Disease Idiopathic fibrosing alveolitis
Variation info
Gene SFTPA2
CLNDBN Idiopathic fibrosing alveolitis, chronic form
Reversed 1
HGVS NC_000010.10:g.81317119A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000014087.24,