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Variant (rsID / SNP)

rs1546960

SCML4

rs1546960 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCML4. Location: chromosome 6, position 108,026,455. The table records no clinical significance for this variant.

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Reference-table entries

SCML4Not classified
Variant type
synonymous_variant
Chromosome / position
6:108026455
HGVS
NM_198081.5,c.1194T>C,p.Pro398Pro
Allele change
Synonymous_P340P

Public references

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