rs104894206

Orientation

minus

Stabilized

minus

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

Make rs104894206(C;T)

Make rs104894206(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

88309176

Gene

CTSC

is a	snp
is	mentioned by
dbSNP	rs104894206
dbSNP (classic)	rs104894206
ClinGen	rs104894206
ebi	rs104894206
HLI	rs104894206
Exac	rs104894206
Gnomad	rs104894206
Varsome	rs104894206
LitVar	rs104894206
Map	rs104894206
PheGenI	rs104894206
Biobank	rs104894206
1000 genomes	rs104894206
hgdp	rs104894206
ensembl	rs104894206
geneview	rs104894206
scholar	rs104894206
google	rs104894206
pharmgkb	rs104894206
gwascentral	rs104894206
openSNP	rs104894206
23andMe	rs104894206
SNPshot	rs104894206
SNPdbe	rs104894206
MSV3d	rs104894206
GWAS Ctlg	rs104894206

Max Magnitude

0

OMIM	602365
Desc
Variant	0001
Related	also

ClinVar
Risk	rs104894206(T;T)
Alt	rs104894206(T;T)
Reference	Rs104894206(C;C)
Significance	Pathogenic
Disease	Papillon-Lefèvre syndrome
Variation	info
Gene	CTSC
CLNDBN	Papillon-Lefèvre syndrome
Reversed	1
HGVS	NC_000011.9:g.88042344G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007712.4,