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Variant (rsID / SNP)

rs76774368

MARCHF7

rs76774368 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MARCHF7. Location: chromosome 2, position 160,604,514. The table records no clinical significance for this variant.

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Reference-table entries

MARCHF7Not classified
Variant type
missense_variant
Chromosome / position
2:160604514
HGVS
NM_001282805.2,c.713C>T,p.Thr238Met
Allele change
Missense_T182M

Public references

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