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Variant (rsID / SNP)

rs2295774

SEC31B

rs2295774 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SEC31B. Location: chromosome 10, position 102,265,847. The table records no clinical significance for this variant.

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Reference-table entries

SEC31BNot classified
Variant type
missense_variant
Chromosome / position
10:102265847
HGVS
NM_015490.4,c.994T>G,p.Ser332Ala
Allele change
Missense_S332A

Public references

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