rs863223922

Orientation

plus

Stabilized

plus

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

Make rs863223922(A;A)

Make rs863223922(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

100989706

Gene	C10orf2, TWNK

is a	snp
is	mentioned by
dbSNP	rs863223922
dbSNP (classic)	rs863223922
ClinGen	rs863223922
ebi	rs863223922
HLI	rs863223922
Exac	rs863223922
Gnomad	rs863223922
Varsome	rs863223922
LitVar	rs863223922
Map	rs863223922
PheGenI	rs863223922
Biobank	rs863223922
1000 genomes	rs863223922
hgdp	rs863223922
ensembl	rs863223922
geneview	rs863223922
scholar	rs863223922
google	rs863223922
pharmgkb	rs863223922
gwascentral	rs863223922
openSNP	rs863223922
23andMe	rs863223922
SNPshot	rs863223922
SNPdbe	rs863223922
MSV3d	rs863223922
GWAS Ctlg	rs863223922

Max Magnitude

0

ClinVar
Risk	rs863223922(A;A)
Alt	rs863223922(A;A)
Reference	Rs863223922(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	C10orf2
CLNDBN	not provided
Reversed	0
HGVS	NC_000010.10:g.102749463G>A
CLNSRC
CLNACC	RCV000197887.1,