rs869312727

Orientation

minus

Stabilized

minus

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

Make rs869312727(C;C)

Make rs869312727(C;T)

Reference

GRCh38.p2 38.2/147

Chromosome

20

Position

6094937

Gene

FERMT1

is a	snp
is	mentioned by
dbSNP	rs869312727
dbSNP (classic)	rs869312727
ClinGen	rs869312727
ebi	rs869312727
HLI	rs869312727
Exac	rs869312727
Gnomad	rs869312727
Varsome	rs869312727
LitVar	rs869312727
Map	rs869312727
PheGenI	rs869312727
Biobank	rs869312727
1000 genomes	rs869312727
hgdp	rs869312727
ensembl	rs869312727
geneview	rs869312727
scholar	rs869312727
google	rs869312727
pharmgkb	rs869312727
gwascentral	rs869312727
openSNP	rs869312727
23andMe	rs869312727
SNPshot	rs869312727
SNPdbe	rs869312727
MSV3d	rs869312727
GWAS Ctlg	rs869312727

Max Magnitude

0

ClinVar
Risk	rs869312727(C;C)
Alt	rs869312727(C;C)
Reference	Rs869312727(T;T)
Significance	Pathogenic
Disease	Kindler's syndrome
Variation	info
Gene	FERMT1
CLNDBN	Kindler's syndrome
Reversed	1
HGVS	NC_000020.10:g.6075584A>G
CLNSRC
CLNACC	RCV000209933.1,