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rs786200930

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786200930(-;-)
Make rs786200930(-;GC)
Make rs786200930(GC;GC)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position127502849
GeneLRSAM1
is asnp
is mentioned by
dbSNPrs786200930
ebirs786200930
HLIrs786200930
Exacrs786200930
Varsomers786200930
Maprs786200930
PheGenIrs786200930
hapmaprs786200930
1000 genomesrs786200930
hgdprs786200930
ensemblrs786200930
gopubmedrs786200930
geneviewrs786200930
scholarrs786200930
googlers786200930
pharmgkbrs786200930
gwascentralrs786200930
openSNPrs786200930
23andMers786200930
23andMe allrs786200930
SNP Nexus

SNPshotrs786200930
SNPdbers786200930
MSV3drs786200930
GWAS Ctlgrs786200930
Max Magnitude0
ClinVar
Risk rs786200930(CG;CG)
Alt rs786200930(CG;CG)
Reference rs786200930(;)
Significance Pathogenic
Disease Charcot-Marie-Tooth disease type 2P Charcot-Marie-Tooth disease
Variation info
Gene LRSAM1
CLNDBN Charcot-Marie-Tooth disease type 2P Charcot-Marie-Tooth disease
Reversed 0
HGVS NC_000009.11:g.130265127_130265128dupGC
CLNSRC OMIM Allelic Variant
CLNACC RCV000023845.4, RCV000192256.1,