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rs397508155

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508155(A;A)
Make rs397508155(A;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117540316
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508155
ebirs397508155
HLIrs397508155
Exacrs397508155
Varsomers397508155
Maprs397508155
PheGenIrs397508155
hapmaprs397508155
1000 genomesrs397508155
hgdprs397508155
ensemblrs397508155
gopubmedrs397508155
geneviewrs397508155
scholarrs397508155
googlers397508155
pharmgkbrs397508155
gwascentralrs397508155
openSNPrs397508155
23andMers397508155
23andMe allrs397508155
SNP Nexus

SNPshotrs397508155
SNPdbers397508155
MSV3drs397508155
GWAS Ctlgrs397508155
Max Magnitude0
ClinVar
Risk rs397508155(A,C,G;A,C,G)
Alt rs397508155(A,C,G;A,C,G)
Reference rs397508155(T;T)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117180370T>A; NC_000007.13:g.117180370T>G
CLNSRC ClinVar
CLNACC RCV000046227.2, RCV000046228.2,