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rs397508638

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508638(-;-)
Make rs397508638(-;A)
Make rs397508638(A;A)
ReferenceGRCh38 38.1/141
Chromosome7
Position117652876
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508638
ebirs397508638
HLIrs397508638
Exacrs397508638
Varsomers397508638
Maprs397508638
PheGenIrs397508638
hapmaprs397508638
1000 genomesrs397508638
hgdprs397508638
ensemblrs397508638
gopubmedrs397508638
geneviewrs397508638
scholarrs397508638
googlers397508638
pharmgkbrs397508638
gwascentralrs397508638
openSNPrs397508638
23andMers397508638
23andMe allrs397508638
SNP Nexus

SNPshotrs397508638
SNPdbers397508638
MSV3drs397508638
GWAS Ctlgrs397508638
Max Magnitude0
ClinVar
Risk rs397508638(A;A)
Alt rs397508638(A;A)
Reference rs397508638(;)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117292930dupA
CLNSRC ClinVar
CLNACC RCV000047027.2,