rs121908796

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar
(G;T)	3	carrier of a cystic fibrosis allele

Make rs121908796(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

117590444

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs121908796
dbSNP (classic)	rs121908796
ClinGen	rs121908796
ebi	rs121908796
HLI	rs121908796
Exac	rs121908796
Gnomad	rs121908796
Varsome	rs121908796
LitVar	rs121908796
Map	rs121908796
PheGenI	rs121908796
Biobank	rs121908796
1000 genomes	rs121908796
hgdp	rs121908796
ensembl	rs121908796
geneview	rs121908796
scholar	rs121908796
google	rs121908796
pharmgkb	rs121908796
gwascentral	rs121908796
openSNP	rs121908796
23andMe	rs121908796
SNPshot	rs121908796
SNPdbe	rs121908796
MSV3d	rs121908796
GWAS Ctlg	rs121908796

Max Magnitude

3

ClinVar
Risk	rs121908796(A;A) rs121908796(T;T)
Alt	rs121908796(A;A) rs121908796(T;T)
Reference	Rs121908796(G;G)
Significance	Pathogenic
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117230498G>A; NC_000007.13:g.117230498G>T
CLNSRC
CLNACC	RCV000046467.2, RCV000046468.3,