rs869312726

Orientation

minus

Stabilized

minus

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

Make rs869312726(A;A)

Make rs869312726(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

20

Position

6097034

Gene

FERMT1

is a	snp
is	mentioned by
dbSNP	rs869312726
dbSNP (classic)	rs869312726
ClinGen	rs869312726
ebi	rs869312726
HLI	rs869312726
Exac	rs869312726
Gnomad	rs869312726
Varsome	rs869312726
LitVar	rs869312726
Map	rs869312726
PheGenI	rs869312726
Biobank	rs869312726
1000 genomes	rs869312726
hgdp	rs869312726
ensembl	rs869312726
geneview	rs869312726
scholar	rs869312726
google	rs869312726
pharmgkb	rs869312726
gwascentral	rs869312726
openSNP	rs869312726
23andMe	rs869312726
SNPshot	rs869312726
SNPdbe	rs869312726
MSV3d	rs869312726
GWAS Ctlg	rs869312726

Max Magnitude

0

ClinVar
Risk	rs869312726(A;A)
Alt	rs869312726(A;A)
Reference	Rs869312726(G;G)
Significance	Pathogenic
Disease	Kindler's syndrome
Variation	info
Gene	FERMT1
CLNDBN	Kindler's syndrome
Reversed	1
HGVS	NC_000020.10:g.6077681C>T
CLNSRC
CLNACC	RCV000209832.1,