rs150239404

Orientation

plus

Stabilized

plus

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

Make rs150239404(A;A)

Make rs150239404(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

100253422

Gene

CWF19L1

is a	snp
is	mentioned by
dbSNP	rs150239404
dbSNP (classic)	rs150239404
ClinGen	rs150239404
ebi	rs150239404
HLI	rs150239404
Exac	rs150239404
Gnomad	rs150239404
Varsome	rs150239404
LitVar	rs150239404
Map	rs150239404
PheGenI	rs150239404
Biobank	rs150239404
1000 genomes	rs150239404
hgdp	rs150239404
ensembl	rs150239404
geneview	rs150239404
scholar	rs150239404
google	rs150239404
pharmgkb	rs150239404
gwascentral	rs150239404
openSNP	rs150239404
23andMe	rs150239404
SNPshot	rs150239404
SNPdbe	rs150239404
MSV3d	rs150239404
GWAS Ctlg	rs150239404

Max Magnitude

0

ClinVar
Risk	rs150239404(A;A)
Alt	rs150239404(A;A)
Reference	Rs150239404(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	CWF19L1
CLNDBN	not provided
Reversed	0
HGVS	NC_000010.10:g.102013179G>A
CLNSRC
CLNACC	RCV000486185.1,