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 CHR:

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EXCLUDE VARIANTS AT VARISNP 		READ DEPTH:

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EXCLUDE ALL VARIANTS PRESENT IN 1000GENOMES 		DBSNP FREQUENCY

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+ Genes 1

Genes:
FAM134B,

+ Genes associated with diseases 1

Genes at Omim

FAM134B,
FAM134B Neuropathy, hereditary sensory and autonomic, type IIB, 613115 (3)

Genes at Clinical Genomics Database

FAM134B,
FAM134B Neuropathy, hereditary sensory and autonomic, type IIB

Genes at HGMD

Summary

Number of Variants: 1
Number of Genes: 1

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FAM134B
Omim - GeneCards - NCBI
Options Individual Chr
 RsId
 Pos
 Qual
 Ref
 Alt
 Filter Gen
 Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View 013 final 5 rs162848
dbSNP Clinvar 		16478200 1221.77 G A PASS 1/1 45 SYNONYMOUS_CODING LOW SILENT 0.67752 0.67750 0.26937 None None None None None None FAM134B|0.118709498|47.64%
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