rs386834228

Orientation

minus

Stabilized

minus

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

Make rs386834228(A;A)

Make rs386834228(A;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

169525949

Gene

F5

is a	snp
is	mentioned by
dbSNP	rs386834228
dbSNP (classic)	rs386834228
ClinGen	rs386834228
ebi	rs386834228
HLI	rs386834228
Exac	rs386834228
Gnomad	rs386834228
Varsome	rs386834228
LitVar	rs386834228
Map	rs386834228
PheGenI	rs386834228
Biobank	rs386834228
1000 genomes	rs386834228
hgdp	rs386834228
ensembl	rs386834228
geneview	rs386834228
scholar	rs386834228
google	rs386834228
pharmgkb	rs386834228
gwascentral	rs386834228
openSNP	rs386834228
23andMe	rs386834228
SNPshot	rs386834228
SNPdbe	rs386834228
MSV3d	rs386834228
GWAS Ctlg	rs386834228

Max Magnitude

0

ClinVar
Risk	rs386834228(A;A)
Alt	rs386834228(A;A)
Reference	Rs386834228(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	F5
CLNDBN	not provided
Reversed	1
HGVS	NC_000001.10:g.169495187C>T
CLNSRC	ClinVar
CLNACC	RCV000049571.1,