rs34006675

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in complete genomics

Make rs34006675(A;A)

Make rs34006675(A;G)

Reference

GRCh38 38.1/141

Chromosome

9

Position

105604218

Gene

FKTN

is a	snp
is	mentioned by
dbSNP	rs34006675
dbSNP (classic)	rs34006675
ClinGen	rs34006675
ebi	rs34006675
HLI	rs34006675
Exac	rs34006675
Gnomad	rs34006675
Varsome	rs34006675
LitVar	rs34006675
Map	rs34006675
PheGenI	rs34006675
Biobank	rs34006675
1000 genomes	rs34006675
hgdp	rs34006675
ensembl	rs34006675
geneview	rs34006675
scholar	rs34006675
google	rs34006675
pharmgkb	rs34006675
gwascentral	rs34006675
openSNP	rs34006675
23andMe	rs34006675
SNPshot	rs34006675
SNPdbe	rs34006675
MSV3d	rs34006675
GWAS Ctlg	rs34006675

GMAF

0.03535

Max Magnitude

0

OMIM	607440
Desc
Variant	0012
Related	also

?	(A;G) (G;G)

ClinVar
Risk	rs34006675(A;A)
Alt	rs34006675(A;A)
Reference	Rs34006675(G;G)
Significance	Non-pathogenic
Disease	Fukuyama congenital muscular dystrophy not specified Walker-Warburg congenital muscular dystrophy
Variation	info
Gene	FKTN
CLNDBN	Fukuyama congenital muscular dystrophy not specified Walker-Warburg congenital muscular dystrophy
Reversed	0
HGVS	NC_000009.11:g.108366499G>A
CLNSRC	HGMD OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000003366.3, RCV000079434.7, RCV000460207.1,