rs121964927

Orientation

plus

Stabilized

plus

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

Make rs121964927(G;T)

Make rs121964927(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

113118716

Gene

F7

is a	snp
is	mentioned by
dbSNP	rs121964927
dbSNP (classic)	rs121964927
ClinGen	rs121964927
ebi	rs121964927
HLI	rs121964927
Exac	rs121964927
Gnomad	rs121964927
Varsome	rs121964927
LitVar	rs121964927
Map	rs121964927
PheGenI	rs121964927
Biobank	rs121964927
1000 genomes	rs121964927
hgdp	rs121964927
ensembl	rs121964927
geneview	rs121964927
scholar	rs121964927
google	rs121964927
pharmgkb	rs121964927
gwascentral	rs121964927
openSNP	rs121964927
23andMe	rs121964927
SNPshot	rs121964927
SNPdbe	rs121964927
MSV3d	rs121964927
GWAS Ctlg	rs121964927

Max Magnitude

0

OMIM	227500
Desc
Variant	0002
Related	also

ClinVar
Risk	rs121964927(T;T)
Alt	rs121964927(T;T)
Reference	Rs121964927(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	F7
CLNDBN	not provided
Reversed	0
HGVS	NC_000013.10:g.113773030G>T
CLNSRC
CLNACC	RCV000254994.1,