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rs397508412

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508412(A;A)
Make rs397508412(A;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117509132
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508412
ebirs397508412
HLIrs397508412
Exacrs397508412
Varsomers397508412
Maprs397508412
PheGenIrs397508412
hapmaprs397508412
1000 genomesrs397508412
hgdprs397508412
ensemblrs397508412
gopubmedrs397508412
geneviewrs397508412
scholarrs397508412
googlers397508412
pharmgkbrs397508412
gwascentralrs397508412
openSNPrs397508412
23andMers397508412
23andMe allrs397508412
SNP Nexus

SNPshotrs397508412
SNPdbers397508412
MSV3drs397508412
GWAS Ctlgrs397508412
Max Magnitude0
ClinVar
Risk rs397508412(A,C,G;A,C,G)
Alt rs397508412(A,C,G;A,C,G)
Reference rs397508412(T;T)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117149186T>A; NC_000007.13:g.117149186T>C; NC_000007.13:g.117149186T>G
CLNSRC ClinVar
CLNACC RCV000046642.2, RCV000046643.2, RCV000046644.2,