rs781906252

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Species

Homo sapiens

Symbol

rs781906252

Category

Variant

Variant type

SNP

Overlaps

RPL36A-HNRNPH2

Location

X:101407947

Nucleotide Change

G>C

Most Severe Consequence

• non coding transcript exon variant

See all consequences

HGVS.g name

• (GRCh38)X:101407947G>C

Show All 5

HGVS.c name

• ENSEMBL:ENST00000409170.3:c.301-3989G>C
• ENSEMBL:ENST00000409338.5:c.178-3989G>C

Show All 7

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences