rs397508162

Orientation

plus

Stabilized

plus

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

Make rs397508162(-;-)

Make rs397508162(-;AT)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117504310

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508162
dbSNP (classic)	rs397508162
ClinGen	rs397508162
ebi	rs397508162
HLI	rs397508162
Exac	rs397508162
Gnomad	rs397508162
Varsome	rs397508162
LitVar	rs397508162
Map	rs397508162
PheGenI	rs397508162
Biobank	rs397508162
1000 genomes	rs397508162
hgdp	rs397508162
ensembl	rs397508162
geneview	rs397508162
scholar	rs397508162
google	rs397508162
pharmgkb	rs397508162
gwascentral	rs397508162
openSNP	rs397508162
23andMe	rs397508162
SNPshot	rs397508162
SNPdbe	rs397508162
MSV3d	rs397508162
GWAS Ctlg	rs397508162

Merged from

Rs397508164

Max Magnitude

0

ClinVar
Risk	rs397508162(-;-) rs397508162(TA;TA)
Alt	rs397508162(-;-) rs397508162(TA;TA)
Reference	Rs397508162(AT;AT)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117144365_117144366delTA
CLNSRC	ClinVar
CLNACC	RCV000046242.4,