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Variant (rsID / SNP)

rs34617762

IGHMBP2

rs34617762 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IGHMBP2. Location: chromosome 11, position 68,673,630. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

IGHMBP2Benign
Clinical significance (as recorded)
Benign/Likely benign
Variant type
single nucleotide variant
Chromosome / position
11:68673630
Cytoband
11q13.3
HGVS
NM_002180.3(IGHMBP2):c.180C>T (p.Tyr60=)
Allele change
Synonymous_Y60Y

Associated conditions / phenotypes

Autosomal recessive distal spinal muscular atrophy 1|Autosomal recessive distal spinal muscular atrophy 1|Charcot-Marie-Tooth disease axonal type 2S|Charcot-Marie-Tooth disease

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.