rs121909618

Orientation

plus

Stabilized

plus

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

Make rs121909618(G;T)

Make rs121909618(T;T)

Reference

GRCh38 38.1/141

Chromosome

4

Position

154565826

Gene

FGB

is a	snp
is	mentioned by
dbSNP	rs121909618
dbSNP (classic)	rs121909618
ClinGen	rs121909618
ebi	rs121909618
HLI	rs121909618
Exac	rs121909618
Gnomad	rs121909618
Varsome	rs121909618
LitVar	rs121909618
Map	rs121909618
PheGenI	rs121909618
Biobank	rs121909618
1000 genomes	rs121909618
hgdp	rs121909618
ensembl	rs121909618
geneview	rs121909618
scholar	rs121909618
google	rs121909618
pharmgkb	rs121909618
gwascentral	rs121909618
openSNP	rs121909618
23andMe	rs121909618
SNPshot	rs121909618
SNPdbe	rs121909618
MSV3d	rs121909618
GWAS Ctlg	rs121909618

Max Magnitude

0

OMIM	134830
Desc
Variant	0005
Related	also

ClinVar
Risk	rs121909618(T;T)
Alt	rs121909618(T;T)
Reference	Rs121909618(G;G)
Significance	Other
Disease	FIBRINOGEN ISE
Variation	info
Gene	FGB
CLNDBN	FIBRINOGEN ISE
Reversed	0
HGVS	NC_000004.11:g.155486978G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000017809.2,