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rs397508207

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508207(G;T)
Make rs397508207(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117559506
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508207
ebirs397508207
HLIrs397508207
Exacrs397508207
Varsomers397508207
Maprs397508207
PheGenIrs397508207
hapmaprs397508207
1000 genomesrs397508207
hgdprs397508207
ensemblrs397508207
gopubmedrs397508207
geneviewrs397508207
scholarrs397508207
googlers397508207
pharmgkbrs397508207
gwascentralrs397508207
openSNPrs397508207
23andMers397508207
23andMe allrs397508207
SNP Nexus

SNPshotrs397508207
SNPdbers397508207
MSV3drs397508207
GWAS Ctlgrs397508207
Max Magnitude0
ClinVar
Risk rs397508207(T;T)
Alt rs397508207(T;T)
Reference rs397508207(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117199560G>T
CLNSRC ClinVar
CLNACC RCV000046302.2,