rs104894198

Orientation

minus

Stabilized

minus

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

Make rs104894198(A;A)

Make rs104894198(A;C)

Reference

GRCh38 38.1/141

Chromosome

11

Position

67365493

Gene	CLCF1, LOC100130987

is a	snp
is	mentioned by
dbSNP	rs104894198
dbSNP (classic)	rs104894198
ClinGen	rs104894198
ebi	rs104894198
HLI	rs104894198
Exac	rs104894198
Gnomad	rs104894198
Varsome	rs104894198
LitVar	rs104894198
Map	rs104894198
PheGenI	rs104894198
Biobank	rs104894198
1000 genomes	rs104894198
hgdp	rs104894198
ensembl	rs104894198
geneview	rs104894198
scholar	rs104894198
google	rs104894198
pharmgkb	rs104894198
gwascentral	rs104894198
openSNP	rs104894198
23andMe	rs104894198
SNPshot	rs104894198
SNPdbe	rs104894198
MSV3d	rs104894198
GWAS Ctlg	rs104894198

Max Magnitude

0

OMIM	607672
Desc
Variant	0001
Related	also

ClinVar
Risk	rs104894198(A;A) rs104894198(T;T)
Alt	rs104894198(A;A) rs104894198(T;T)
Reference	Rs104894198(C;C)
Significance	Pathogenic
Disease	Cold-induced sweating syndrome 2
Variation	info
Gene	CLCF1 LOC100130987
CLNDBN	Cold-induced sweating syndrome 2
Reversed	1
HGVS	NC_000011.9:g.67132964G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000003064.2,