rs397508504

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs397508504(C;C)

Make rs397508504(C;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117610669

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508504
dbSNP (classic)	rs397508504
ClinGen	rs397508504
ebi	rs397508504
HLI	rs397508504
Exac	rs397508504
Gnomad	rs397508504
Varsome	rs397508504
LitVar	rs397508504
Map	rs397508504
PheGenI	rs397508504
Biobank	rs397508504
1000 genomes	rs397508504
hgdp	rs397508504
ensembl	rs397508504
geneview	rs397508504
scholar	rs397508504
google	rs397508504
pharmgkb	rs397508504
gwascentral	rs397508504
openSNP	rs397508504
23andMe	rs397508504
SNPshot	rs397508504
SNPdbe	rs397508504
MSV3d	rs397508504
GWAS Ctlg	rs397508504

Max Magnitude

0

ClinVar
Risk	rs397508504(C;C) rs397508504(T;T)
Alt	rs397508504(C;C) rs397508504(T;T)
Reference	Rs397508504(G;G)
Significance	Untested
Disease	Cystic fibrosis not specified
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis not specified
Reversed	0
HGVS	NC_000007.13:g.117250723G>C; NC_000007.13:g.117250723G>T
CLNSRC	ClinVar
CLNACC	RCV000046790.2, RCV000307800.1,