rs371546359

Orientation

plus

Stabilized

plus

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

Make rs371546359(A;A)

Make rs371546359(A;T)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

69419606

Gene

NFU1

is a	snp
is	mentioned by
dbSNP	rs371546359
dbSNP (classic)	rs371546359
ClinGen	rs371546359
ebi	rs371546359
HLI	rs371546359
Exac	rs371546359
Gnomad	rs371546359
Varsome	rs371546359
LitVar	rs371546359
Map	rs371546359
PheGenI	rs371546359
Biobank	rs371546359
1000 genomes	rs371546359
hgdp	rs371546359
ensembl	rs371546359
geneview	rs371546359
scholar	rs371546359
google	rs371546359
pharmgkb	rs371546359
gwascentral	rs371546359
openSNP	rs371546359
23andMe	rs371546359
SNPshot	rs371546359
SNPdbe	rs371546359
MSV3d	rs371546359
GWAS Ctlg	rs371546359

Max Magnitude

0

ClinVar
Risk	rs371546359(A;A)
Alt	rs371546359(A;A)
Reference	Rs371546359(T;T)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	NFU1
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.69646738T>A
CLNSRC
CLNACC	RCV000198803.1,