rs797044939

Orientation

minus

Stabilized

minus

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

Make rs797044939(A;G)

Make rs797044939(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

19

Position

49061477

Gene

NTF4

is a	snp
is	mentioned by
dbSNP	rs797044939
dbSNP (classic)	rs797044939
ClinGen	rs797044939
ebi	rs797044939
HLI	rs797044939
Exac	rs797044939
Gnomad	rs797044939
Varsome	rs797044939
LitVar	rs797044939
Map	rs797044939
PheGenI	rs797044939
Biobank	rs797044939
1000 genomes	rs797044939
hgdp	rs797044939
ensembl	rs797044939
geneview	rs797044939
scholar	rs797044939
google	rs797044939
pharmgkb	rs797044939
gwascentral	rs797044939
openSNP	rs797044939
23andMe	rs797044939
SNPshot	rs797044939
SNPdbe	rs797044939
MSV3d	rs797044939
GWAS Ctlg	rs797044939

Max Magnitude

0

ClinVar
Risk	rs797044939(G;G)
Alt	rs797044939(G;G)
Reference	Rs797044939(A;A)
Significance	Probable-Pathogenic
Disease	Inborn genetic diseases
Variation	info
Gene	NTF4
CLNDBN	Inborn genetic diseases
Reversed	1
HGVS	NC_000019.9:g.49564734T>C
CLNSRC
CLNACC	RCV000190785.1,