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Variant (rsID / SNP)

rs117750891

CALHM4

rs117750891 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CALHM4. Location: chromosome 6, position 116,864,998. The table records no clinical significance for this variant.

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Reference-table entries

CALHM4Not classified
Variant type
missense_variant
Chromosome / position
6:116864998
HGVS
NM_001256888.3,c.22G>A,p.Glu8Lys
Allele change
Silent

Public references

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