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rs767302772

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs767302772(C;T)
Make rs767302772(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position151650316
GeneNEB
is asnp
is mentioned by
dbSNPrs767302772
ebirs767302772
HLIrs767302772
Exacrs767302772
Varsomers767302772
Maprs767302772
PheGenIrs767302772
hapmaprs767302772
1000 genomesrs767302772
hgdprs767302772
ensemblrs767302772
gopubmedrs767302772
geneviewrs767302772
scholarrs767302772
googlers767302772
pharmgkbrs767302772
gwascentralrs767302772
openSNPrs767302772
23andMers767302772
23andMe allrs767302772
SNP Nexus

SNPshotrs767302772
SNPdbers767302772
MSV3drs767302772
GWAS Ctlgrs767302772
Max Magnitude0
ClinVar
Risk rs767302772(A,T;A,T)
Alt rs767302772(A,T;A,T)
Reference rs767302772(C;C)
Significance Probable-Pathogenic
Disease Nemaline myopathy 2
Variation info
Gene NEB
CLNDBN Nemaline myopathy 2
Reversed 0
HGVS NC_000002.11:g.152506830C>T
CLNSRC
CLNACC RCV000227541.1,