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rs773457070

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs773457070(G;T)
Make rs773457070(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome18
Position6955368
GeneLAMA1, LOC101927188
is asnp
is mentioned by
dbSNPrs773457070
dbSNP (classic)rs773457070
ClinGenrs773457070
ebirs773457070
HLIrs773457070
Exacrs773457070
Gnomadrs773457070
Varsomers773457070
LitVarrs773457070
Maprs773457070
PheGenIrs773457070
Biobankrs773457070
1000 genomesrs773457070
hgdprs773457070
ensemblrs773457070
geneviewrs773457070
scholarrs773457070
googlers773457070
pharmgkbrs773457070
gwascentralrs773457070
openSNPrs773457070
23andMers773457070
SNPshotrs773457070
SNPdbers773457070
MSV3drs773457070
GWAS Ctlgrs773457070
Max Magnitude0
ClinVar
Risk rs773457070(T;T)
Alt rs773457070(T;T)
Reference Rs773457070(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC101927188 LAMA1
CLNDBN not provided
Reversed 0
HGVS NC_000018.9:g.6955367G>T
CLNSRC
CLNACC RCV000413473.1,