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rs397508613

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508613(A;A)
Make rs397508613(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117642542
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508613
ebirs397508613
HLIrs397508613
Exacrs397508613
Varsomers397508613
Maprs397508613
PheGenIrs397508613
hapmaprs397508613
1000 genomesrs397508613
hgdprs397508613
ensemblrs397508613
gopubmedrs397508613
geneviewrs397508613
scholarrs397508613
googlers397508613
pharmgkbrs397508613
gwascentralrs397508613
openSNPrs397508613
23andMers397508613
23andMe allrs397508613
SNP Nexus

SNPshotrs397508613
SNPdbers397508613
MSV3drs397508613
GWAS Ctlgrs397508613
Max Magnitude0
ClinVar
Risk rs397508613(A;A)
Alt rs397508613(A;A)
Reference rs397508613(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117282596G>A
CLNSRC ClinVar
CLNACC RCV000046989.2,