rs121964942

Orientation

plus

Stabilized

plus

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

Make rs121964942(A;A)

Make rs121964942(A;G)

Reference

GRCh38 38.1/141

Chromosome

13

Position

113149014

Gene

F10

is a	snp
is	mentioned by
dbSNP	rs121964942
dbSNP (classic)	rs121964942
ClinGen	rs121964942
ebi	rs121964942
HLI	rs121964942
Exac	rs121964942
Gnomad	rs121964942
Varsome	rs121964942
LitVar	rs121964942
Map	rs121964942
PheGenI	rs121964942
Biobank	rs121964942
1000 genomes	rs121964942
hgdp	rs121964942
ensembl	rs121964942
geneview	rs121964942
scholar	rs121964942
google	rs121964942
pharmgkb	rs121964942
gwascentral	rs121964942
openSNP	rs121964942
23andMe	rs121964942
SNPshot	rs121964942
SNPdbe	rs121964942
MSV3d	rs121964942
GWAS Ctlg	rs121964942

Max Magnitude

0

OMIM	227600
Desc
Variant	0008
Related	also

ClinVar
Risk	rs121964942(A;A)
Alt	rs121964942(A;A)
Reference	Rs121964942(G;G)
Significance	Untested
Disease
Variation	info
Gene	F10
CLNDBN
Reversed	0
HGVS	NC_000013.10:g.113803328G>A
CLNSRC
CLNACC