rs28445840

Orientation

plus

Stabilized

plus

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

Make rs28445840(A;A)

Make rs28445840(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

22

Position

36864918

Gene	LOC107985578, NCF4

is a	snp
is	mentioned by
dbSNP	rs28445840
dbSNP (classic)	rs28445840
ClinGen	rs28445840
ebi	rs28445840
HLI	rs28445840
Exac	rs28445840
Gnomad	rs28445840
Varsome	rs28445840
LitVar	rs28445840
Map	rs28445840
PheGenI	rs28445840
Biobank	rs28445840
1000 genomes	rs28445840
hgdp	rs28445840
ensembl	rs28445840
geneview	rs28445840
scholar	rs28445840
google	rs28445840
pharmgkb	rs28445840
gwascentral	rs28445840
openSNP	rs28445840
23andMe	rs28445840
SNPshot	rs28445840
SNPdbe	rs28445840
MSV3d	rs28445840
GWAS Ctlg	rs28445840

Max Magnitude

0

ClinVar
Risk	rs28445840(A;A)
Alt	rs28445840(A;A)
Reference	Rs28445840(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	NCF4
CLNDBN	not provided
Reversed	0
HGVS	NC_000022.10:g.37260960G>A
CLNSRC
CLNACC	RCV000488142.1,