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rs397508287

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508287(G;T)
Make rs397508287(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117590408
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508287
ebirs397508287
HLIrs397508287
Exacrs397508287
Varsomers397508287
Maprs397508287
PheGenIrs397508287
hapmaprs397508287
1000 genomesrs397508287
hgdprs397508287
ensemblrs397508287
gopubmedrs397508287
geneviewrs397508287
scholarrs397508287
googlers397508287
pharmgkbrs397508287
gwascentralrs397508287
openSNPrs397508287
23andMers397508287
23andMe allrs397508287
SNP Nexus

SNPshotrs397508287
SNPdbers397508287
MSV3drs397508287
GWAS Ctlgrs397508287
Max Magnitude0
ClinVar
Risk rs397508287(T;T)
Alt rs397508287(T;T)
Reference rs397508287(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117230462G>T
CLNSRC ClinVar
CLNACC RCV000046449.2,