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Variant (rsID / SNP)

rs2301802

SRRM2

rs2301802 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SRRM2. Location: chromosome 16, position 2,818,161. The table records no clinical significance for this variant.

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Reference-table entries

SRRM2Not classified
Variant type
synonymous_variant
Chromosome / position
16:2818161
HGVS
NM_016333.4,c.7632T>C,p.Ser2544Ser
Allele change
Synonymous_S2544S

Public references

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