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rs397508642

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508642(A;A)
Make rs397508642(A;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117652889
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508642
ebirs397508642
HLIrs397508642
Exacrs397508642
Varsomers397508642
Maprs397508642
PheGenIrs397508642
hapmaprs397508642
1000 genomesrs397508642
hgdprs397508642
ensemblrs397508642
gopubmedrs397508642
geneviewrs397508642
scholarrs397508642
googlers397508642
pharmgkbrs397508642
gwascentralrs397508642
openSNPrs397508642
23andMers397508642
23andMe allrs397508642
SNP Nexus

SNPshotrs397508642
SNPdbers397508642
MSV3drs397508642
GWAS Ctlgrs397508642
Max Magnitude0
ClinVar
Risk rs397508642(A;A)
Alt rs397508642(A;A)
Reference rs397508642(T;T)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117292943T>A
CLNSRC ClinVar
CLNACC RCV000047033.2,