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rs397508808

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508808(C;T)
Make rs397508808(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117536672
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508808
ebirs397508808
HLIrs397508808
Exacrs397508808
Varsomers397508808
Maprs397508808
PheGenIrs397508808
hapmaprs397508808
1000 genomesrs397508808
hgdprs397508808
ensemblrs397508808
gopubmedrs397508808
geneviewrs397508808
scholarrs397508808
googlers397508808
pharmgkbrs397508808
gwascentralrs397508808
openSNPrs397508808
23andMers397508808
23andMe allrs397508808
SNP Nexus

SNPshotrs397508808
SNPdbers397508808
MSV3drs397508808
GWAS Ctlgrs397508808
Max Magnitude0
ClinVar
Risk rs397508808(T;T)
Alt rs397508808(T;T)
Reference rs397508808(C;C)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117176726C>T
CLNSRC ClinVar
CLNACC RCV000047274.2,