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rs397508311

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508311(C;C)
Make rs397508311(C;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117591996
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508311
ebirs397508311
HLIrs397508311
Exacrs397508311
Varsomers397508311
Maprs397508311
PheGenIrs397508311
hapmaprs397508311
1000 genomesrs397508311
hgdprs397508311
ensemblrs397508311
gopubmedrs397508311
geneviewrs397508311
scholarrs397508311
googlers397508311
pharmgkbrs397508311
gwascentralrs397508311
openSNPrs397508311
23andMers397508311
23andMe allrs397508311
SNP Nexus

SNPshotrs397508311
SNPdbers397508311
MSV3drs397508311
GWAS Ctlgrs397508311
Max Magnitude0
ClinVar
Risk rs397508311(C;C)
Alt rs397508311(C;C)
Reference rs397508311(T;T)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232050T>C
CLNSRC ClinVar
CLNACC RCV000046490.2,