rs386834226

Orientation

minus

Stabilized

minus

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

Make rs386834226(-;A)

Make rs386834226(A;A)

Reference

GRCh38 38.1/141

Chromosome

1

Position

169541903

Gene

F5

is a	snp
is	mentioned by
dbSNP	rs386834226
dbSNP (classic)	rs386834226
ClinGen	rs386834226
ebi	rs386834226
HLI	rs386834226
Exac	rs386834226
Gnomad	rs386834226
Varsome	rs386834226
LitVar	rs386834226
Map	rs386834226
PheGenI	rs386834226
Biobank	rs386834226
1000 genomes	rs386834226
hgdp	rs386834226
ensembl	rs386834226
geneview	rs386834226
scholar	rs386834226
google	rs386834226
pharmgkb	rs386834226
gwascentral	rs386834226
openSNP	rs386834226
23andMe	rs386834226
SNPshot	rs386834226
SNPdbe	rs386834226
MSV3d	rs386834226
GWAS Ctlg	rs386834226

Max Magnitude

0

ClinVar
Risk	rs386834226(A;A)
Alt	rs386834226(A;A)
Reference	Rs386834226(-;-)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	F5
CLNDBN	not provided
Reversed	1
HGVS	NC_000001.10:g.169511142dupT
CLNSRC	ClinVar
CLNACC	RCV000049569.1,