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rs397508633

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508633(-;-)
Make rs397508633(-;T)
Make rs397508633(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117652858
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508633
ebirs397508633
HLIrs397508633
Exacrs397508633
Varsomers397508633
Maprs397508633
PheGenIrs397508633
hapmaprs397508633
1000 genomesrs397508633
hgdprs397508633
ensemblrs397508633
gopubmedrs397508633
geneviewrs397508633
scholarrs397508633
googlers397508633
pharmgkbrs397508633
gwascentralrs397508633
openSNPrs397508633
23andMers397508633
23andMe allrs397508633
SNP Nexus

SNPshotrs397508633
SNPdbers397508633
MSV3drs397508633
GWAS Ctlgrs397508633
Max Magnitude0
ClinVar
Risk rs397508633(T;T)
Alt rs397508633(T;T)
Reference rs397508633(;)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117292913dupT
CLNSRC ClinVar
CLNACC RCV000047020.2,