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rs397508506

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508506(A;A)
Make rs397508506(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117611580
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508506
ebirs397508506
HLIrs397508506
Exacrs397508506
Varsomers397508506
Maprs397508506
PheGenIrs397508506
hapmaprs397508506
1000 genomesrs397508506
hgdprs397508506
ensemblrs397508506
gopubmedrs397508506
geneviewrs397508506
scholarrs397508506
googlers397508506
pharmgkbrs397508506
gwascentralrs397508506
openSNPrs397508506
23andMers397508506
23andMe allrs397508506
SNP Nexus

SNPshotrs397508506
SNPdbers397508506
MSV3drs397508506
GWAS Ctlgrs397508506
Max Magnitude0
ClinVar
Risk rs397508506(A;A)
Alt rs397508506(A;A)
Reference rs397508506(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117251634G>A
CLNSRC ClinVar
CLNACC RCV000046793.2,