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rs397508611

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508611(G;G)
Make rs397508611(G;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117531005
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508611
ebirs397508611
HLIrs397508611
Exacrs397508611
Varsomers397508611
Maprs397508611
PheGenIrs397508611
hapmaprs397508611
1000 genomesrs397508611
hgdprs397508611
ensemblrs397508611
gopubmedrs397508611
geneviewrs397508611
scholarrs397508611
googlers397508611
pharmgkbrs397508611
gwascentralrs397508611
openSNPrs397508611
23andMers397508611
23andMe allrs397508611
SNP Nexus

SNPshotrs397508611
SNPdbers397508611
MSV3drs397508611
GWAS Ctlgrs397508611
Max Magnitude0
ClinVar
Risk rs397508611(G;G)
Alt rs397508611(G;G)
Reference rs397508611(T;T)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117171059T>G
CLNSRC ClinVar
CLNACC RCV000046987.2,