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rs397508637

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;A) 3 carrier of a cystic fibrosis allele
(A;A) 0 common in clinvar


Make rs397508637(-;-)
ReferenceGRCh38 38.1/141
Chromosome7
Position117652876
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508637
ebirs397508637
HLIrs397508637
Exacrs397508637
Varsomers397508637
Maprs397508637
PheGenIrs397508637
hapmaprs397508637
1000 genomesrs397508637
hgdprs397508637
ensemblrs397508637
gopubmedrs397508637
geneviewrs397508637
scholarrs397508637
googlers397508637
pharmgkbrs397508637
gwascentralrs397508637
openSNPrs397508637
23andMers397508637
23andMe allrs397508637
SNP Nexus

SNPshotrs397508637
SNPdbers397508637
MSV3drs397508637
GWAS Ctlgrs397508637
Max Magnitude3
ClinVar
Risk rs397508637(;)
Alt rs397508637(;)
Reference rs397508637(A;A)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117292930delA
CLNSRC CFTR2
CLNACC RCV000047026.3,