rs104893885

Orientation

minus

Stabilized

minus

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

Make rs104893885(G;T)

Make rs104893885(T;T)

Reference

GRCh38 38.1/141

Chromosome

5

Position

44388366

Gene	FGF10, FGF10-AS1

is a	snp
is	mentioned by
dbSNP	rs104893885
dbSNP (classic)	rs104893885
ClinGen	rs104893885
ebi	rs104893885
HLI	rs104893885
Exac	rs104893885
Gnomad	rs104893885
Varsome	rs104893885
LitVar	rs104893885
Map	rs104893885
PheGenI	rs104893885
Biobank	rs104893885
1000 genomes	rs104893885
hgdp	rs104893885
ensembl	rs104893885
geneview	rs104893885
scholar	rs104893885
google	rs104893885
pharmgkb	rs104893885
gwascentral	rs104893885
openSNP	rs104893885
23andMe	rs104893885
SNPshot	rs104893885
SNPdbe	rs104893885
MSV3d	rs104893885
GWAS Ctlg	rs104893885

Max Magnitude

0

OMIM	602115
Desc
Variant	0003
Related	also

ClinVar
Risk	rs104893885(T;T)
Alt	rs104893885(T;T)
Reference	Rs104893885(G;G)
Significance	Pathogenic
Disease	Levy-Hollister syndrome
Variation	info
Gene	FGF10-AS1 LOC101927075 FGF10
CLNDBN	Levy-Hollister syndrome
Reversed	1
HGVS	NC_000005.9:g.44388468C>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000007966.2,