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rs397508431

From SNPedia

Cystic Fibrosis related
Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(-;AG) 3 carrier of a cystic fibrosis allele
Make rs397508431(-;-)
Make rs397508431(AG;AG)
ReferenceGRCh38 38.1/141
Chromosome7
Position117603638
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508431
ebirs397508431
HLIrs397508431
Exacrs397508431
Varsomers397508431
Maprs397508431
PheGenIrs397508431
hapmaprs397508431
1000 genomesrs397508431
hgdprs397508431
ensemblrs397508431
gopubmedrs397508431
geneviewrs397508431
scholarrs397508431
googlers397508431
pharmgkbrs397508431
gwascentralrs397508431
openSNPrs397508431
23andMers397508431
23andMe allrs397508431
SNP Nexus

SNPshotrs397508431
SNPdbers397508431
MSV3drs397508431
GWAS Ctlgrs397508431
Max Magnitude3

Cystic fibrosis; c.2764_2765insAG, p.Val922Glufs

named i5011656 by 23andMe

ClinVar
Risk rs397508431(GA;GA)
Alt rs397508431(GA;GA)
Reference rs397508431(;)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117243691_117243692dupAG
CLNSRC CFTR2
CLNACC RCV000046684.3,