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rs397508302

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508302(A;T)
Make rs397508302(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117591959
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508302
ebirs397508302
HLIrs397508302
Exacrs397508302
Varsomers397508302
Maprs397508302
PheGenIrs397508302
hapmaprs397508302
1000 genomesrs397508302
hgdprs397508302
ensemblrs397508302
gopubmedrs397508302
geneviewrs397508302
scholarrs397508302
googlers397508302
pharmgkbrs397508302
gwascentralrs397508302
openSNPrs397508302
23andMers397508302
23andMe allrs397508302
SNP Nexus

SNPshotrs397508302
SNPdbers397508302
MSV3drs397508302
GWAS Ctlgrs397508302
Max Magnitude0
ClinVar
Risk rs397508302(T;T)
Alt rs397508302(T;T)
Reference rs397508302(A;A)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232013A>T
CLNSRC ClinVar
CLNACC RCV000046476.2,