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Variant (rsID / SNP)

rs10206850

THSD7B

rs10206850 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to THSD7B. Location: chromosome 2, position 138,420,996. The table records no clinical significance for this variant.

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Reference-table entries

THSD7BNot classified
Variant type
missense_variant
Chromosome / position
2:138420996
HGVS
NM_001316349.2,c.4502A>G,p.Lys1501Arg
Allele change
Missense_K1501R

Public references

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