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rs796065332

From SNPedia

Orientationplus
Geno Mag Summary
(AAATGATTGAAAA;AAATGATTGAAAA) 0 common in clinvar
Make rs796065332(AAATGATTGAAAA;TG)
Make rs796065332(TG;TG)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position117536652
GeneCFTR
is asnp
is mentioned by
dbSNPrs796065332
ebirs796065332
HLIrs796065332
Exacrs796065332
Varsomers796065332
Maprs796065332
PheGenIrs796065332
hapmaprs796065332
1000 genomesrs796065332
hgdprs796065332
ensemblrs796065332
gopubmedrs796065332
geneviewrs796065332
scholarrs796065332
googlers796065332
pharmgkbrs796065332
gwascentralrs796065332
openSNPrs796065332
23andMers796065332
23andMe allrs796065332
SNP Nexus

SNPshotrs796065332
SNPdbers796065332
MSV3drs796065332
GWAS Ctlgrs796065332
Max Magnitude0
ClinVar
Risk rs796065332(TG;TG)
Alt rs796065332(TG;TG)
Reference rs796065332(AAATGATTGAAAA;AAATGATTGAAAA)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117176706_117176718delAAATGATTGAAAAinsTG
CLNSRC
CLNACC RCV000179761.1,