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Variant (rsID / SNP)

rs3766400

THEMIS2

rs3766400 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to THEMIS2. Location: chromosome 1, position 28,209,366. The table records no clinical significance for this variant.

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Reference-table entries

THEMIS2Not classified
Variant type
missense_variant
Chromosome / position
1:28209366
HGVS
NM_001105556.3,c.1531A>G,p.Lys511Glu
Allele change
Missense_K511E

Public references

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