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rs397508231

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508231(C;C)
Make rs397508231(C;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117559657
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508231
ebirs397508231
HLIrs397508231
Exacrs397508231
Varsomers397508231
Maprs397508231
PheGenIrs397508231
hapmaprs397508231
1000 genomesrs397508231
hgdprs397508231
ensemblrs397508231
gopubmedrs397508231
geneviewrs397508231
scholarrs397508231
googlers397508231
pharmgkbrs397508231
gwascentralrs397508231
openSNPrs397508231
23andMers397508231
23andMe allrs397508231
SNP Nexus

SNPshotrs397508231
SNPdbers397508231
MSV3drs397508231
GWAS Ctlgrs397508231
Max Magnitude0
ClinVar
Risk rs397508231(C;C)
Alt rs397508231(C;C)
Reference rs397508231(T;T)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117199711T>C
CLNSRC ClinVar
CLNACC RCV000046348.2,