rs121964940

Orientation

plus

Stabilized

plus

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

Make rs121964940(C;T)

Make rs121964940(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

113149197

Gene	F10, LOC102724474

is a	snp
is	mentioned by
dbSNP	rs121964940
dbSNP (classic)	rs121964940
ClinGen	rs121964940
ebi	rs121964940
HLI	rs121964940
Exac	rs121964940
Gnomad	rs121964940
Varsome	rs121964940
LitVar	rs121964940
Map	rs121964940
PheGenI	rs121964940
Biobank	rs121964940
1000 genomes	rs121964940
hgdp	rs121964940
ensembl	rs121964940
geneview	rs121964940
scholar	rs121964940
google	rs121964940
pharmgkb	rs121964940
gwascentral	rs121964940
openSNP	rs121964940
23andMe	rs121964940
SNPshot	rs121964940
SNPdbe	rs121964940
MSV3d	rs121964940
GWAS Ctlg	rs121964940

Max Magnitude

0

OMIM	227600
Desc
Variant	0004
Related	also

ClinVar
Risk	rs121964940(T;T)
Alt	rs121964940(T;T)
Reference	Rs121964940(C;C)
Significance	Untested
Disease
Variation	info
Gene	F10
CLNDBN
Reversed	0
HGVS	NC_000013.10:g.113803511C>T
CLNSRC
CLNACC