rs137853235

Orientation

minus

Stabilized

minus

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

Make rs137853235(A;A)

Make rs137853235(A;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

81752250

Gene

HGF

is a	snp
is	mentioned by
dbSNP	rs137853235
dbSNP (classic)	rs137853235
ClinGen	rs137853235
ebi	rs137853235
HLI	rs137853235
Exac	rs137853235
Gnomad	rs137853235
Varsome	rs137853235
LitVar	rs137853235
Map	rs137853235
PheGenI	rs137853235
Biobank	rs137853235
1000 genomes	rs137853235
hgdp	rs137853235
ensembl	rs137853235
geneview	rs137853235
scholar	rs137853235
google	rs137853235
pharmgkb	rs137853235
gwascentral	rs137853235
openSNP	rs137853235
23andMe	rs137853235
SNPshot	rs137853235
SNPdbe	rs137853235
MSV3d	rs137853235
GWAS Ctlg	rs137853235

Max Magnitude

0

OMIM	142409
Desc
Variant	0001
Related	also

ClinVar
Risk	rs137853235(A;A)
Alt	rs137853235(A;A)
Reference	Rs137853235(G;G)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	HGF
CLNDBN	Deafness, autosomal recessive 39
Reversed	1
HGVS	NC_000007.13:g.81381566C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000016089.22,