rs386834227

Orientation

minus

Stabilized

minus

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

Make rs386834227(A;A)

Make rs386834227(A;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

169529635

Gene

F5

is a	snp
is	mentioned by
dbSNP	rs386834227
dbSNP (classic)	rs386834227
ClinGen	rs386834227
ebi	rs386834227
HLI	rs386834227
Exac	rs386834227
Gnomad	rs386834227
Varsome	rs386834227
LitVar	rs386834227
Map	rs386834227
PheGenI	rs386834227
Biobank	rs386834227
1000 genomes	rs386834227
hgdp	rs386834227
ensembl	rs386834227
geneview	rs386834227
scholar	rs386834227
google	rs386834227
pharmgkb	rs386834227
gwascentral	rs386834227
openSNP	rs386834227
23andMe	rs386834227
SNPshot	rs386834227
SNPdbe	rs386834227
MSV3d	rs386834227
GWAS Ctlg	rs386834227

Max Magnitude

0

ClinVar
Risk	rs386834227(A;A)
Alt	rs386834227(A;A)
Reference	Rs386834227(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	F5
CLNDBN	not provided
Reversed	1
HGVS	NC_000001.10:g.169498873C>T
CLNSRC	ClinVar
CLNACC	RCV000049570.1,