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Variant (rsID / SNP)

rs2275996

IGHMBP2

rs2275996 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IGHMBP2. Location: chromosome 11, position 68,705,820. Clinical significance in the table: Benign.

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Reference-table entries

IGHMBP2Benign
Clinical significance (as recorded)
Benign
Variant type
single nucleotide variant
Chromosome / position
11:68705820
Cytoband
11q13.3
HGVS
NM_002180.3(IGHMBP2):c.2782G>A (p.Glu928Lys)
Allele change
Missense_E928K

Associated conditions / phenotypes

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