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rs121908803

From SNPedia

Cystic Fibrosis related
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 3 carrier of a cystic fibrosis allele
Make rs121908803(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117535281
GeneCFTR
is asnp
is mentioned by
dbSNPrs121908803
ebirs121908803
HLIrs121908803
Exacrs121908803
Varsomers121908803
Maprs121908803
PheGenIrs121908803
hapmaprs121908803
1000 genomesrs121908803
hgdprs121908803
ensemblrs121908803
gopubmedrs121908803
geneviewrs121908803
scholarrs121908803
googlers121908803
pharmgkbrs121908803
gwascentralrs121908803
openSNPrs121908803
23andMers121908803
23andMe allrs121908803
SNP Nexus

SNPshotrs121908803
SNPdbers121908803
MSV3drs121908803
GWAS Ctlgrs121908803
Max Magnitude3

Cystic fibrosis; c.613C>T, Pro205Ser or P205S

named i5010966 by 23andMe

ClinVar
Risk rs121908803(T;T)
Alt rs121908803(T;T)
Reference rs121908803(C;C)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117175335C>T
CLNSRC CFTR2
CLNACC RCV000056400.3,