rs869312725

Orientation

minus

Stabilized

minus

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

Make rs869312725(A;A)

Make rs869312725(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

20

Position

6097523

Gene

FERMT1

is a	snp
is	mentioned by
dbSNP	rs869312725
dbSNP (classic)	rs869312725
ClinGen	rs869312725
ebi	rs869312725
HLI	rs869312725
Exac	rs869312725
Gnomad	rs869312725
Varsome	rs869312725
LitVar	rs869312725
Map	rs869312725
PheGenI	rs869312725
Biobank	rs869312725
1000 genomes	rs869312725
hgdp	rs869312725
ensembl	rs869312725
geneview	rs869312725
scholar	rs869312725
google	rs869312725
pharmgkb	rs869312725
gwascentral	rs869312725
openSNP	rs869312725
23andMe	rs869312725
SNPshot	rs869312725
SNPdbe	rs869312725
MSV3d	rs869312725
GWAS Ctlg	rs869312725

Max Magnitude

0

ClinVar
Risk	rs869312725(A;A)
Alt	rs869312725(A;A)
Reference	Rs869312725(G;G)
Significance	Pathogenic
Disease	Kindler's syndrome
Variation	info
Gene	FERMT1
CLNDBN	Kindler's syndrome
Reversed	1
HGVS	NC_000020.10:g.6078170C>T
CLNSRC
CLNACC	RCV000209916.1,