rs397508138

Orientation

plus

Stabilized

plus

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

Make rs397508138(G;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117540236

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508138
dbSNP (classic)	rs397508138
ClinGen	rs397508138
ebi	rs397508138
HLI	rs397508138
Exac	rs397508138
Gnomad	rs397508138
Varsome	rs397508138
LitVar	rs397508138
Map	rs397508138
PheGenI	rs397508138
Biobank	rs397508138
1000 genomes	rs397508138
hgdp	rs397508138
ensembl	rs397508138
geneview	rs397508138
scholar	rs397508138
google	rs397508138
pharmgkb	rs397508138
gwascentral	rs397508138
openSNP	rs397508138
23andMe	rs397508138
SNPshot	rs397508138
SNPdbe	rs397508138
MSV3d	rs397508138
GWAS Ctlg	rs397508138

Max Magnitude

3

ClinVar
Risk	rs397508138(G;G)
Alt	rs397508138(G;G)
Reference	Rs397508138(-;-)
Significance	Pathogenic
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117180290_117180291insG
CLNSRC	CFTR2
CLNACC	RCV000046194.3,