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rs397508774

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508774(-;-)
Make rs397508774(-;T)
Make rs397508774(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117535310
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508774
ebirs397508774
HLIrs397508774
Exacrs397508774
Varsomers397508774
Maprs397508774
PheGenIrs397508774
hapmaprs397508774
1000 genomesrs397508774
hgdprs397508774
ensemblrs397508774
gopubmedrs397508774
geneviewrs397508774
scholarrs397508774
googlers397508774
pharmgkbrs397508774
gwascentralrs397508774
openSNPrs397508774
23andMers397508774
23andMe allrs397508774
SNP Nexus

SNPshotrs397508774
SNPdbers397508774
MSV3drs397508774
GWAS Ctlgrs397508774
Max Magnitude0
ClinVar
Risk rs397508774(T;T)
Alt rs397508774(T;T)
Reference rs397508774(;)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117175364_117175365insT
CLNSRC ClinVar
CLNACC RCV000047226.2,