rs6063

minus

Geno	Mag	Summary
(A;A)	2
(A;G)		None
(G;G)	0	common

Reference

GRCh38 38.1/142

Chromosome

4

Position

154609725

Gene

FGG

is a	snp
is	mentioned by
dbSNP	rs6063
dbSNP (classic)	rs6063
ClinGen	rs6063
ebi	rs6063
HLI	rs6063
Exac	rs6063
Gnomad	rs6063
Varsome	rs6063
LitVar	rs6063
Map	rs6063
PheGenI	rs6063
Biobank	rs6063
1000 genomes	rs6063
hgdp	rs6063
ensembl	rs6063
geneview	rs6063
scholar	rs6063
google	rs6063
pharmgkb	rs6063
gwascentral	rs6063
openSNP	rs6063
23andMe	rs6063
SNPshot	rs6063
SNPdbe	rs6063
MSV3d	rs6063
GWAS Ctlg	rs6063

GMAF

0.006428

Max Magnitude

2

?

(A;A) (A;G) (G;G)

28

OMIM	134850
Desc	FIBRINOGEN MILANO XII, DIGENIC
Variant	0018
Related	also

This is the first snp to experiment with the watson alignment.

Overview of the Watson Alignment

r_gnl|ti|1767110221/265-275 AGAGCGGGCTT
gnl|ti|1846769777/267-277   AGAGCGGGCTT
gnl|ti|1832408368/258-268   NGAGCGGTCTT
gnl|ti|1797000559/116-126   AGAGCGGGCTT
gnl|dbSNP|rs6063/96-106     AGAGCRGGCTT
r_gnl|ti|1817651632/252-262 AAAAGGAAACT
                              *       *

ClinVar
Risk	Rs6063(A;A)
Alt	Rs6063(A;A)
Reference	Rs6063(G;G)
Significance	Pathogenic
Disease	Fibrinogen Milano XII
Variation	info
Gene	FGG
CLNDBN	Fibrinogen Milano XII, digenic
Reversed	1
HGVS	NC_000004.11:g.155530877C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017800.4,