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rs397508824

From SNPedia

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


Make rs397508824(-;-)
ReferenceGRCh38 38.1/141
Chromosome7
Position117540217
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508824
ebirs397508824
HLIrs397508824
Exacrs397508824
Varsomers397508824
Maprs397508824
PheGenIrs397508824
hapmaprs397508824
1000 genomesrs397508824
hgdprs397508824
ensemblrs397508824
gopubmedrs397508824
geneviewrs397508824
scholarrs397508824
googlers397508824
pharmgkbrs397508824
gwascentralrs397508824
openSNPrs397508824
23andMers397508824
23andMe allrs397508824
SNP Nexus

SNPshotrs397508824
SNPdbers397508824
MSV3drs397508824
GWAS Ctlgrs397508824
Max Magnitude3
ClinVar
Risk rs397508824(;)
Alt rs397508824(;)
Reference rs397508824(A;A)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117180271delA
CLNSRC CFTR2
CLNACC RCV000047303.3,