rs869312723

Orientation

minus

Stabilized

minus

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

Make rs869312723(-;-)

Make rs869312723(-;T)

Reference

GRCh38.p2 38.2/147

Chromosome

20

Position

6115823

Gene

FERMT1

is a	snp
is	mentioned by
dbSNP	rs869312723
dbSNP (classic)	rs869312723
ClinGen	rs869312723
ebi	rs869312723
HLI	rs869312723
Exac	rs869312723
Gnomad	rs869312723
Varsome	rs869312723
LitVar	rs869312723
Map	rs869312723
PheGenI	rs869312723
Biobank	rs869312723
1000 genomes	rs869312723
hgdp	rs869312723
ensembl	rs869312723
geneview	rs869312723
scholar	rs869312723
google	rs869312723
pharmgkb	rs869312723
gwascentral	rs869312723
openSNP	rs869312723
23andMe	rs869312723
SNPshot	rs869312723
SNPdbe	rs869312723
MSV3d	rs869312723
GWAS Ctlg	rs869312723

Max Magnitude

0

ClinVar
Risk	rs869312723(-;-)
Alt	rs869312723(-;-)
Reference	Rs869312723(T;T)
Significance	Pathogenic
Disease	Kindler's syndrome
Variation	info
Gene	FERMT1
CLNDBN	Kindler's syndrome
Reversed	1
HGVS	NC_000020.10:g.6096470delA
CLNSRC
CLNACC	RCV000209899.1,